Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
This document outlines the key concepts and learning objectives for Chapter 16 on acid-base equilibria. It covers the acid-base properties of weak acids and bases in solution, including acid-ionization equilibria, polyprotic acids, and base-ionization equilibria. It also discusses acid-base properties of salt solutions, the common ion effect, buffers, and acid-base titration curves. The chapter provides the necessary background for students to write and balance acid-base reactions, determine equilibrium constants and concentrations of species, and perform acid-base calculations.
This document discusses acids and bases, including:
- The Arrhenius definition of acids and bases as substances that increase H+ or OH- ions in water.
- The Brรธnsted-Lowry definition of acids as proton donors and bases as proton acceptors.
- Conjugate acid-base pairs that differ by the presence or absence of a proton.
- Amphoteric substances that can act as both acids and bases, such as water.
- The pH scale for measuring the concentration of hydrogen ions in a solution.
- Strong acids and bases that fully dissociate in water versus weak acids and bases that only partially dissociate.
This document discusses several topics related to aqueous solutions and chemical equilibria, including:
1) Buffers and how they resist changes in pH when acids or bases are added. The NH3/NH4+ system is used as an example buffer.
2) Solubility equilibria and how the solubility of salts can be calculated using Ksp. Common ion and precipitation effects are also covered.
3) Precipitation of insoluble salts and how to determine which salt precipitates first based on differences in Ksp values.
IB Chemistry on Free radical substitution, Addition and Nucleophilic substitu...Lawrence kok
ย
This document describes various classes of organic compounds including alkanes, alkenes, alcohols, esters, and their properties. Alkanes are saturated hydrocarbons with the general formula CnH2n+2. Alkenes are unsaturated hydrocarbons containing carbon-carbon double bonds with the general formula CnH2n. Alcohols contain an -OH functional group and have the general formula CnH2n+1OH. Esters are formed from the condensation reaction between carboxylic acids and alcohols, producing water as a byproduct. Common chemical reactions for each class are also outlined such as combustion, addition, oxidation, and esterification
This document discusses several concepts related to buffers, including:
1) Calculating the pH of an acetate buffer with given concentrations. The pH is calculated to be 4.67.
2) Choosing an appropriate buffer to achieve a target pH of 4.30 from given options based on their pKa values. Acetate is chosen.
3) Calculating the acid concentration needed for a 0.100 M base concentration to achieve the target pH. The acid concentration is calculated to be 0.28 M.
This document outlines the key concepts and learning objectives for Chapter 17, which covers solubility equilibria and complex-ion equilibria. The chapter will examine how to determine solubility product constants (Ksp) and use them to calculate solubility. It will also explore how the common ion effect and pH can impact solubility. The chapter will then discuss the formation of complex ions and how they relate to solubility and precipitation. It concludes by looking at applications to qualitative metal ion analysis.
Here are the ratios [HA]/[A-] required for each system to yield a pH of 4.30:
Acetic acid (pKa = 4.76): [HA]/[A-] = 1
Benzoic acid (pKa = 4.19): [HA]/[A-] = 1
Phthalic acid (pKa = 2.89): [HA]/[A-] is not possible since the pKa is too low.
The optimal system is acetic acid/sodium acetate since it has a pKa closest to the desired pH of 4.30. This system allows a ratio of [HA]/[A-] = 1, which provides maximum buffering
IB Chemistry Nucleophilic Substitution, SN1, SN2 and protic solventLawrence kok
ย
This document describes organic functional groups including alkanes, alkenes, alcohols, esters, and their characteristic properties and reactions. Alkanes are saturated hydrocarbons with single carbon-carbon bonds and have low reactivity. Alkenes are unsaturated hydrocarbons with carbon-carbon double bonds and undergo addition reactions more readily than alkanes. Alcohols contain an -OH group and can be oxidized to aldehydes, ketones, or carboxylic acids. Esters are formed from the condensation reaction between carboxylic acids and alcohols, producing water.
This document outlines the key concepts and learning objectives for Chapter 16 on acid-base equilibria. It covers the acid-base properties of weak acids and bases in solution, including acid-ionization equilibria, polyprotic acids, and base-ionization equilibria. It also discusses acid-base properties of salt solutions, the common ion effect, buffers, and acid-base titration curves. The chapter provides the necessary background for students to write and balance acid-base reactions, determine equilibrium constants and concentrations of species, and perform acid-base calculations.
This document discusses acids and bases, including:
- The Arrhenius definition of acids and bases as substances that increase H+ or OH- ions in water.
- The Brรธnsted-Lowry definition of acids as proton donors and bases as proton acceptors.
- Conjugate acid-base pairs that differ by the presence or absence of a proton.
- Amphoteric substances that can act as both acids and bases, such as water.
- The pH scale for measuring the concentration of hydrogen ions in a solution.
- Strong acids and bases that fully dissociate in water versus weak acids and bases that only partially dissociate.
This document discusses several topics related to aqueous solutions and chemical equilibria, including:
1) Buffers and how they resist changes in pH when acids or bases are added. The NH3/NH4+ system is used as an example buffer.
2) Solubility equilibria and how the solubility of salts can be calculated using Ksp. Common ion and precipitation effects are also covered.
3) Precipitation of insoluble salts and how to determine which salt precipitates first based on differences in Ksp values.
IB Chemistry on Free radical substitution, Addition and Nucleophilic substitu...Lawrence kok
ย
This document describes various classes of organic compounds including alkanes, alkenes, alcohols, esters, and their properties. Alkanes are saturated hydrocarbons with the general formula CnH2n+2. Alkenes are unsaturated hydrocarbons containing carbon-carbon double bonds with the general formula CnH2n. Alcohols contain an -OH functional group and have the general formula CnH2n+1OH. Esters are formed from the condensation reaction between carboxylic acids and alcohols, producing water as a byproduct. Common chemical reactions for each class are also outlined such as combustion, addition, oxidation, and esterification
This document discusses several concepts related to buffers, including:
1) Calculating the pH of an acetate buffer with given concentrations. The pH is calculated to be 4.67.
2) Choosing an appropriate buffer to achieve a target pH of 4.30 from given options based on their pKa values. Acetate is chosen.
3) Calculating the acid concentration needed for a 0.100 M base concentration to achieve the target pH. The acid concentration is calculated to be 0.28 M.
This document outlines the key concepts and learning objectives for Chapter 17, which covers solubility equilibria and complex-ion equilibria. The chapter will examine how to determine solubility product constants (Ksp) and use them to calculate solubility. It will also explore how the common ion effect and pH can impact solubility. The chapter will then discuss the formation of complex ions and how they relate to solubility and precipitation. It concludes by looking at applications to qualitative metal ion analysis.
Here are the ratios [HA]/[A-] required for each system to yield a pH of 4.30:
Acetic acid (pKa = 4.76): [HA]/[A-] = 1
Benzoic acid (pKa = 4.19): [HA]/[A-] = 1
Phthalic acid (pKa = 2.89): [HA]/[A-] is not possible since the pKa is too low.
The optimal system is acetic acid/sodium acetate since it has a pKa closest to the desired pH of 4.30. This system allows a ratio of [HA]/[A-] = 1, which provides maximum buffering
IB Chemistry Nucleophilic Substitution, SN1, SN2 and protic solventLawrence kok
ย
This document describes organic functional groups including alkanes, alkenes, alcohols, esters, and their characteristic properties and reactions. Alkanes are saturated hydrocarbons with single carbon-carbon bonds and have low reactivity. Alkenes are unsaturated hydrocarbons with carbon-carbon double bonds and undergo addition reactions more readily than alkanes. Alcohols contain an -OH group and can be oxidized to aldehydes, ketones, or carboxylic acids. Esters are formed from the condensation reaction between carboxylic acids and alcohols, producing water.
This document discusses several key topics regarding bases:
1. The hydroxides of Group 1 and 2 elements are strong bases, with NaOH and KOH being common laboratory reagents. The alkaline earth hydroxides have low solubility.
2. Calculating the pH of a solution involves determining the hydroxide ion concentration from any reacting species. A 5.0x10-2 M NaOH solution has a pH of 12.70.
3. Many bases other than hydroxides can produce hydroxide ions through reaction with water, such as ammonia. Calculations for weak bases are similar to weak acids.
4. Salts can behave as acids or bases depending on
IB Chemistry on Arrhenius, Bronsted Lowry Conjugate Acid Base Pair and Lewis ...Lawrence kok
ย
The document defines different types of acids and bases. Brรธnsted-Lowry acids are proton donors that donate a proton to a Brรธnsted-Lowry base, which accepts the proton. Every acid has a conjugate base and every base has a conjugate acid. The conjugate acid has one more hydrogen ion than the conjugate base. Strong acids form weak conjugate bases that do not readily accept protons back, while weak acids form strong conjugate bases that can accept protons. Strong bases form weak conjugate acids that do not readily donate protons, while weak bases form strong conjugate acids that can donate protons. Some substances can act as both acids and bases depending on conditions and are called amphiprotic or amphoteric. Lewis acids are
The document discusses different definitions of acids and bases, including:
1) Arrhenius definitions - acids produce H+ ions in water, bases produce OH- ions. Limited to aqueous solutions.
2) Bronsted-Lowry definitions - acids are H+ donors, bases are H+ acceptors. Acids and bases always come in pairs when reacting.
3) pH scale is used to express acidity because [H+] is usually very small. pH decreases as [H+] increases exponentially. Common substances are classified as acidic, basic, or neutral based on their pH.
IB Chemistry on Nucleophilic Substitution, SN1, SN2 and protic solventLawrence kok
ย
This document provides a tutorial on organic chemistry reactions, specifically nucleophilic substitution reactions (SN1 and SN2) and the reactivity of functional groups. It discusses the properties and reactions of alkanes, alkenes, alcohols, aldehydes, ketones, carboxylic acids, and esters. Key reactions covered include combustion, halogenation, oxidation, esterification, and polymerization. Reaction mechanisms and conditions are explained for common transformations of functional groups like alcohol oxidation and ester synthesis.
This document discusses Bronsted-Lowry acid-base chemistry. It defines Bronsted-Lowry acids as proton donors and bases as proton acceptors. It explains that conjugate acids are formed by adding a proton to a base and conjugate bases are formed by removing a proton from an acid. Several examples of conjugate acid-base pairs are given. The document also states that the stronger the acid, the weaker its conjugate base, and the stronger the base, the weaker its conjugate acid. It describes how the position of equilibrium favors transfer of a proton to the stronger base. Finally, it provides the autoionization reaction of water and defines the ion product constant, Kw, for water.
This document provides an overview of acids, bases, and salts. It discusses several acid-base theories including:
- Arrhenius theory which defines acids as producing H+ ions and bases as producing OH- ions.
- Brรธnsted-Lowry theory which defines acids as proton donors and bases as proton acceptors.
It also describes properties such as:
- Strong vs weak acids and bases based on extent of ionization.
- Mono-, di-, and triprotic acids based on the number of protons donated.
- pH and pKa scales for representing acidity and acid strength.
- Hydrolysis of salt solutions and how it affects pH depending on
The document discusses various concepts related to aqueous equilibria including:
1) The common ion effect where adding a strong electrolyte containing a common ion with a weak electrolyte decreases the ionization of the weak electrolyte.
2) Buffers and how they resist pH changes through reactions of the weak acid/base with added strong acid or base.
3) Solubility products (Ksp) and how solubility is affected by factors like common ions, pH, and complex ion formation.
This document provides an overview of acids and bases for an AP Chemistry course. It begins with definitions of acids and bases according to Arrhenius, Brรธnsted-Lowry, and Lewis theories. It then distinguishes between strong and weak acids/bases, as well as concentrated and dilute solutions. Conjugate acids and bases are defined. Equilibrium concepts such as acid dissociation constants (Ka) and base dissociation constants (Kb) are introduced, and their relationships to strength are explained. The autoionization of water and the water dissociation constant (Kw) are covered. Finally, the logarithmic pH scale is defined.
B sc_I_General chemistry U-II Ionic equilibria in aqueous solution Rai University
ย
This document provides an overview of acids, bases, and pH. It defines acids and bases according to Arrhenius, Brรธnsted-Lowry, and Lewis theories. Acids are substances that produce H+ ions in water or donate protons in reactions, while bases produce OH- ions or accept protons. The document also discusses acid and base strength, pH, self-ionization of water, and using pH to calculate hydrogen or hydroxide ion concentrations. Common examples like acids in orange juice and blood pH are provided.
2012 topic 18 1 calculations involving acids and basesDavid Young
ย
The document provides information about acid-base calculations including:
1) It defines the ionic product constant of water (Kw) and how it depends on temperature.
2) It shows how to calculate the hydroxide ion concentration and pH of pure water given the Kw value at a certain temperature.
3) It discusses the dissociation reactions of weak acids and bases and how they do not dissociate 100% like strong acids and bases.
This document discusses acid-base chemistry and provides information on different acid-base theories, acid and base strength, pH calculations, and polyprotic acids. It includes definitions, examples, and practice problems related to these topics. Key points covered include the Arrhenius, Brรธnsted-Lowry, and Lewis theories of acids and bases, definitions of strong and weak acids/bases, calculations for pH and pOH, and the stepwise dissociation of polyprotic acids. Practice problems are provided throughout for calculating pH, pOH, and acid/base ionization constants.
This document discusses weak acid-base equilibria according to Bronsted-Lowry theory. It defines acids and bases as proton donors and acceptors, respectively. Conjugate acid-base pairs are introduced. Strong acids and bases completely dissociate in water, while weak acids and bases only partially dissociate. The ionic product of water, Kw, relates the concentrations of H+ and OH- ions in solution. Equations are provided to calculate the pH of solutions containing weak acids or bases using their respective acid or base dissociation constants, Ka or Kb.
The document discusses several key topics regarding acids and bases:
1. Group 1 and 2 hydroxides such as LiOH, NaOH, and Ca(OH)2 are strong bases. NaOH and KOH are common laboratory reagents while alkaline earth hydroxides have low solubility.
2. Calculating pH involves determining the hydroxide ion concentration from solubility equations or acid/base equilibria. Examples show calculating the pH of NaOH and NH3 solutions.
3. Many bases like NH3 produce hydroxide ions when dissolved in water by reacting with water. The acid dissociation constant Kb describes this reaction.
4. Polyprotic acids dissociate
IB Chemistry on Homologous series and functional groups of organic moleculesLawrence kok
ย
The document discusses organic functional groups and their IUPAC nomenclature rules. It defines classes of organic compounds such as alkanes, alkenes, alkynes, alcohols, ethers, ketones, aldehydes, carboxylic acids, esters, amides, amines, nitriles and haloalkanes based on their functional groups. It provides examples and molecular formulas for different functional groups and discusses IUPAC nomenclature rules for systematically naming organic compounds including identifying the parent chain, functional group, substituents and their positions.
IB Chemistry on Acid Base, pH Scale and Ionic Product Water, KwLawrence kok
ย
This document defines different types of acids and bases and their properties. It discusses Bronsted-Lowry acids and bases, which are defined by their ability to donate or accept protons. Arrhenius acids and bases are defined by their ability to produce H+ or OH- ions when dissolved in water. Lewis acids are electron acceptors while Lewis bases are electron donors. Strong acids fully dissociate in water producing H+ ions, while weak acids only partially dissociate. Concentrated acids have more moles of solute per liter than diluted acids. The pH scale is used to measure acidity, with lower pH indicating more acidic solutions.
This document summarizes key reactions of alkenes, including addition reactions and mechanisms. It discusses catalytic hydrogenation, electrophilic additions, hydroboration-oxidation, carbene and radical additions, polymerization, and the roles of alkenes in natural products like pheromones. It also provides examples of alkene reactions in nature, like steroid synthesis, and commercial applications, such as in polyethylene and margarine production.
This document provides an overview of acid-base theories and key concepts such as:
[1] Arrhenius and Brรธnsted-Lowry definitions of acids and bases. Acids donate protons while bases accept protons.
[2] Water can act as both an acid and a base in different reactions due to its amphiprotic nature.
[3] Equilibria involving proton transfers favor the reaction where the proton moves to the stronger base. The position of equilibrium is determined by relative acid and base strengths.
IB Chemistry on Mass Spectrometry, Index Hydrogen Deficiency and IsotopesLawrence kok
ย
This document provides a tutorial on mass spectrometry, isotopes identification, and index hydrogen deficiency (IHD). It defines IHD as the degree of unsaturation in a molecule, and explains how to calculate IHD based on the number of double bonds, rings, or other functional groups present. It also discusses how the presence of isotopes affects relative atomic mass calculations. Mass spectrometry techniques are described for identifying isotopes and abundances, calculating relative atomic masses, determining molecular structure, and distinguishing between structural isomers.
This document provides an overview of additional aspects of acid-base equilibria, including:
1. Important relations for pH, pOH, Ka, and Kb calculations.
2. Steps for calculating pH, pKa, [H+], Ka for acids or bases, including distinguishing between strong and weak acids/bases.
3. Steps for calculating pH for mixtures of acids and bases, including considerations for salt solutions, buffer solutions, and calculating pH changes upon adding small amounts of acid or base to a buffer.
The document is a scoring guideline for a 2009 AP Chemistry exam question relating to halogen oxoacids. It provides the question text and outlines the points earned for each part. The question tests students' understanding of acid strength, Lewis structures, acid/base equilibria, and buffer solutions. It requires calculations of Ka values, hydrolysis constants, ion concentrations, and pH.
Chemistry AP Free-Response Questions Form B 2009UCLA
ย
The document is the 2009 AP Chemistry free-response questions. It includes:
1) An introduction to the College Board, the non-profit organization that administers the AP exam.
2) Information about the 2009 AP Chemistry exam, including standard reduction potentials, equations, and constants that may be useful for the free-response questions.
3) The first three free-response questions asking students to perform calculations related to weak acid/base equilibrium, rate law determination from experimental data, and thermochemistry.
This document discusses several key topics regarding bases:
1. The hydroxides of Group 1 and 2 elements are strong bases, with NaOH and KOH being common laboratory reagents. The alkaline earth hydroxides have low solubility.
2. Calculating the pH of a solution involves determining the hydroxide ion concentration from any reacting species. A 5.0x10-2 M NaOH solution has a pH of 12.70.
3. Many bases other than hydroxides can produce hydroxide ions through reaction with water, such as ammonia. Calculations for weak bases are similar to weak acids.
4. Salts can behave as acids or bases depending on
IB Chemistry on Arrhenius, Bronsted Lowry Conjugate Acid Base Pair and Lewis ...Lawrence kok
ย
The document defines different types of acids and bases. Brรธnsted-Lowry acids are proton donors that donate a proton to a Brรธnsted-Lowry base, which accepts the proton. Every acid has a conjugate base and every base has a conjugate acid. The conjugate acid has one more hydrogen ion than the conjugate base. Strong acids form weak conjugate bases that do not readily accept protons back, while weak acids form strong conjugate bases that can accept protons. Strong bases form weak conjugate acids that do not readily donate protons, while weak bases form strong conjugate acids that can donate protons. Some substances can act as both acids and bases depending on conditions and are called amphiprotic or amphoteric. Lewis acids are
The document discusses different definitions of acids and bases, including:
1) Arrhenius definitions - acids produce H+ ions in water, bases produce OH- ions. Limited to aqueous solutions.
2) Bronsted-Lowry definitions - acids are H+ donors, bases are H+ acceptors. Acids and bases always come in pairs when reacting.
3) pH scale is used to express acidity because [H+] is usually very small. pH decreases as [H+] increases exponentially. Common substances are classified as acidic, basic, or neutral based on their pH.
IB Chemistry on Nucleophilic Substitution, SN1, SN2 and protic solventLawrence kok
ย
This document provides a tutorial on organic chemistry reactions, specifically nucleophilic substitution reactions (SN1 and SN2) and the reactivity of functional groups. It discusses the properties and reactions of alkanes, alkenes, alcohols, aldehydes, ketones, carboxylic acids, and esters. Key reactions covered include combustion, halogenation, oxidation, esterification, and polymerization. Reaction mechanisms and conditions are explained for common transformations of functional groups like alcohol oxidation and ester synthesis.
This document discusses Bronsted-Lowry acid-base chemistry. It defines Bronsted-Lowry acids as proton donors and bases as proton acceptors. It explains that conjugate acids are formed by adding a proton to a base and conjugate bases are formed by removing a proton from an acid. Several examples of conjugate acid-base pairs are given. The document also states that the stronger the acid, the weaker its conjugate base, and the stronger the base, the weaker its conjugate acid. It describes how the position of equilibrium favors transfer of a proton to the stronger base. Finally, it provides the autoionization reaction of water and defines the ion product constant, Kw, for water.
This document provides an overview of acids, bases, and salts. It discusses several acid-base theories including:
- Arrhenius theory which defines acids as producing H+ ions and bases as producing OH- ions.
- Brรธnsted-Lowry theory which defines acids as proton donors and bases as proton acceptors.
It also describes properties such as:
- Strong vs weak acids and bases based on extent of ionization.
- Mono-, di-, and triprotic acids based on the number of protons donated.
- pH and pKa scales for representing acidity and acid strength.
- Hydrolysis of salt solutions and how it affects pH depending on
The document discusses various concepts related to aqueous equilibria including:
1) The common ion effect where adding a strong electrolyte containing a common ion with a weak electrolyte decreases the ionization of the weak electrolyte.
2) Buffers and how they resist pH changes through reactions of the weak acid/base with added strong acid or base.
3) Solubility products (Ksp) and how solubility is affected by factors like common ions, pH, and complex ion formation.
This document provides an overview of acids and bases for an AP Chemistry course. It begins with definitions of acids and bases according to Arrhenius, Brรธnsted-Lowry, and Lewis theories. It then distinguishes between strong and weak acids/bases, as well as concentrated and dilute solutions. Conjugate acids and bases are defined. Equilibrium concepts such as acid dissociation constants (Ka) and base dissociation constants (Kb) are introduced, and their relationships to strength are explained. The autoionization of water and the water dissociation constant (Kw) are covered. Finally, the logarithmic pH scale is defined.
B sc_I_General chemistry U-II Ionic equilibria in aqueous solution Rai University
ย
This document provides an overview of acids, bases, and pH. It defines acids and bases according to Arrhenius, Brรธnsted-Lowry, and Lewis theories. Acids are substances that produce H+ ions in water or donate protons in reactions, while bases produce OH- ions or accept protons. The document also discusses acid and base strength, pH, self-ionization of water, and using pH to calculate hydrogen or hydroxide ion concentrations. Common examples like acids in orange juice and blood pH are provided.
2012 topic 18 1 calculations involving acids and basesDavid Young
ย
The document provides information about acid-base calculations including:
1) It defines the ionic product constant of water (Kw) and how it depends on temperature.
2) It shows how to calculate the hydroxide ion concentration and pH of pure water given the Kw value at a certain temperature.
3) It discusses the dissociation reactions of weak acids and bases and how they do not dissociate 100% like strong acids and bases.
This document discusses acid-base chemistry and provides information on different acid-base theories, acid and base strength, pH calculations, and polyprotic acids. It includes definitions, examples, and practice problems related to these topics. Key points covered include the Arrhenius, Brรธnsted-Lowry, and Lewis theories of acids and bases, definitions of strong and weak acids/bases, calculations for pH and pOH, and the stepwise dissociation of polyprotic acids. Practice problems are provided throughout for calculating pH, pOH, and acid/base ionization constants.
This document discusses weak acid-base equilibria according to Bronsted-Lowry theory. It defines acids and bases as proton donors and acceptors, respectively. Conjugate acid-base pairs are introduced. Strong acids and bases completely dissociate in water, while weak acids and bases only partially dissociate. The ionic product of water, Kw, relates the concentrations of H+ and OH- ions in solution. Equations are provided to calculate the pH of solutions containing weak acids or bases using their respective acid or base dissociation constants, Ka or Kb.
The document discusses several key topics regarding acids and bases:
1. Group 1 and 2 hydroxides such as LiOH, NaOH, and Ca(OH)2 are strong bases. NaOH and KOH are common laboratory reagents while alkaline earth hydroxides have low solubility.
2. Calculating pH involves determining the hydroxide ion concentration from solubility equations or acid/base equilibria. Examples show calculating the pH of NaOH and NH3 solutions.
3. Many bases like NH3 produce hydroxide ions when dissolved in water by reacting with water. The acid dissociation constant Kb describes this reaction.
4. Polyprotic acids dissociate
IB Chemistry on Homologous series and functional groups of organic moleculesLawrence kok
ย
The document discusses organic functional groups and their IUPAC nomenclature rules. It defines classes of organic compounds such as alkanes, alkenes, alkynes, alcohols, ethers, ketones, aldehydes, carboxylic acids, esters, amides, amines, nitriles and haloalkanes based on their functional groups. It provides examples and molecular formulas for different functional groups and discusses IUPAC nomenclature rules for systematically naming organic compounds including identifying the parent chain, functional group, substituents and their positions.
IB Chemistry on Acid Base, pH Scale and Ionic Product Water, KwLawrence kok
ย
This document defines different types of acids and bases and their properties. It discusses Bronsted-Lowry acids and bases, which are defined by their ability to donate or accept protons. Arrhenius acids and bases are defined by their ability to produce H+ or OH- ions when dissolved in water. Lewis acids are electron acceptors while Lewis bases are electron donors. Strong acids fully dissociate in water producing H+ ions, while weak acids only partially dissociate. Concentrated acids have more moles of solute per liter than diluted acids. The pH scale is used to measure acidity, with lower pH indicating more acidic solutions.
This document summarizes key reactions of alkenes, including addition reactions and mechanisms. It discusses catalytic hydrogenation, electrophilic additions, hydroboration-oxidation, carbene and radical additions, polymerization, and the roles of alkenes in natural products like pheromones. It also provides examples of alkene reactions in nature, like steroid synthesis, and commercial applications, such as in polyethylene and margarine production.
This document provides an overview of acid-base theories and key concepts such as:
[1] Arrhenius and Brรธnsted-Lowry definitions of acids and bases. Acids donate protons while bases accept protons.
[2] Water can act as both an acid and a base in different reactions due to its amphiprotic nature.
[3] Equilibria involving proton transfers favor the reaction where the proton moves to the stronger base. The position of equilibrium is determined by relative acid and base strengths.
IB Chemistry on Mass Spectrometry, Index Hydrogen Deficiency and IsotopesLawrence kok
ย
This document provides a tutorial on mass spectrometry, isotopes identification, and index hydrogen deficiency (IHD). It defines IHD as the degree of unsaturation in a molecule, and explains how to calculate IHD based on the number of double bonds, rings, or other functional groups present. It also discusses how the presence of isotopes affects relative atomic mass calculations. Mass spectrometry techniques are described for identifying isotopes and abundances, calculating relative atomic masses, determining molecular structure, and distinguishing between structural isomers.
This document provides an overview of additional aspects of acid-base equilibria, including:
1. Important relations for pH, pOH, Ka, and Kb calculations.
2. Steps for calculating pH, pKa, [H+], Ka for acids or bases, including distinguishing between strong and weak acids/bases.
3. Steps for calculating pH for mixtures of acids and bases, including considerations for salt solutions, buffer solutions, and calculating pH changes upon adding small amounts of acid or base to a buffer.
The document is a scoring guideline for a 2009 AP Chemistry exam question relating to halogen oxoacids. It provides the question text and outlines the points earned for each part. The question tests students' understanding of acid strength, Lewis structures, acid/base equilibria, and buffer solutions. It requires calculations of Ka values, hydrolysis constants, ion concentrations, and pH.
Chemistry AP Free-Response Questions Form B 2009UCLA
ย
The document is the 2009 AP Chemistry free-response questions. It includes:
1) An introduction to the College Board, the non-profit organization that administers the AP exam.
2) Information about the 2009 AP Chemistry exam, including standard reduction potentials, equations, and constants that may be useful for the free-response questions.
3) The first three free-response questions asking students to perform calculations related to weak acid/base equilibrium, rate law determination from experimental data, and thermochemistry.
This document discusses weak bases and how they react with water to form the conjugate acid and hydroxide ions. It defines the base dissociation constant Kb and explains how it refers to the equilibrium of a base reacting with water. It provides examples of calculating the concentration of hydroxide ions produced from a weak base solution and calculating Kb or Ka values for conjugate acid-base pairs using known constants. The document also discusses how the properties of salt solutions are determined by the constituent ions and how buffers resist changes in pH upon addition of acids or bases.
This document provides instructions for students to complete pre-lab calculations to design a buffer solution for a chemistry lab experiment. It specifies that students must determine the acid/salt pair to use based on an assigned pH value between 1 and 8. It then outlines the calculations needed to determine the amounts of acid and salt to measure out, including molar concentrations and masses, using the dilution equation and Henderson-Hasselbalch formula. Students are reminded to show their work and have their calculations verified before starting the experiment.
AP Chemistry Chapter 17 Sample ExercisesJane Hamze
ย
This document provides two sample exercises for calculating pH at different points in a titration reaction between a strong acid (HCl) and a strong base (NaOH).
In the first exercise, the pH is calculated when 49.0 mL of 0.1 M NaOH has been added to 50.0 mL of 0.1 M HCl. At this point, just before the equivalence point, the pH is determined by the small amount of unreacted HCl.
In the second exercise, the pH is calculated when 51.0 mL of NaOH has been added, just past the equivalence point. Here the pH is determined by the small excess of OH- ions remaining after the HCl is fully
Chemical Structure: Chemical Bonding. Molecular Orbitalsulcerd
ย
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Structure of Matter. Atoms โ the building blocks of matterulcerd
ย
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical and Physical Properties: Isotopes and Forensic Scienceulcerd
ย
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Chemical Bonding. Homonuclear Covalent Bondsulcerd
ย
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical and Physical Properties: Practical Sessionulcerd
ย
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Chemical Bonding. Properties of Coordination Compounds ulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Chemical Bonding. Ionic, Metallic & Coordinate Bondsulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
The document summarizes key concepts about chemical equilibrium including:
1) Chemical equilibrium occurs when the forward and reverse reactions of a chemical reaction proceed at the same rate.
2) At equilibrium, the concentrations of reactants and products remain constant.
3) The equilibrium constant, K, provides a measure of how far a reaction proceeds towards products or reactants.
4) Changing conditions like concentration, temperature, or pressure will shift equilibrium to counteract the change according to Le Chรขtelier's principle.
Chemical Structure: Chemical Nomenclature. Inorganic Compoundsulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical and Physical Properties: Chemical vs. Physical Propertiesulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Lect w8 152 - ka and kb calculations_abbrev_algchelss
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This document summarizes key concepts about acids and bases from a general chemistry unit, including:
1) Methods for calculating pH of acids and bases, whether strong or weak, by considering chemical equilibrium and ionization constants.
2) Factors that influence acid/base strength such as electronegativity, inductive effects, and resonance stabilization.
3) Properties of salts in solution, with examples of salts producing acidic, basic, or neutral solutions.
This document covers various topics related to chemical equilibrium including:
1. Irreversible and reversible reactions, and examples of each.
2. Types of equilibrium including homogeneous, heterogeneous, physical, and chemical equilibrium.
3. The law of mass action and how equilibrium constants are calculated.
4. How changing conditions like temperature, pressure, and concentration affects chemical equilibria.
5. Additional topics like acid-base theories, buffer solutions, and solubility products are also briefly discussed.
- Chemical equilibrium is reached when the rates of the forward and reverse reactions of a reversible reaction are equal. At equilibrium, the concentrations of reactants and products no longer change over time.
- The equilibrium constant, K, is a measure of the extent to which a reaction favors products or reactants at equilibrium. If K is large, products are favored. If K is small, reactants are favored.
- Le Chatelier's principle states that if a system at equilibrium is disturbed, the equilibrium will shift in a direction that counteracts the applied change.
The document discusses acids, bases, and pH. It explains that acids donate H+ ions while bases accept H+ ions. Common acids include HCl and carbonic acid, while NaOH is a strong base. Neutralization reactions between acids and bases produce water and salts. Buffers resist changes in pH. The pH scale ranges from 0-14 with acidic solutions having a pH below 7 and basic solutions above 7. The carbonate buffering system and carbon dioxide system in the ocean help regulate ocean pH. Increasing carbon dioxide absorption is lowering ocean pH and threatening marine organisms with calcium carbonate shells or skeletons.
Lect w7 152_abbrev_ intro to acids and bases_algchelss
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This document provides an overview of acids and bases, including:
- Water can act as both an acid and a base in chemical reactions.
- The autoionization of water establishes an equilibrium expression relating [H3O+] and [OH-].
- Adding acids or bases shifts the equilibrium by changing [H3O+] or [OH-] while maintaining the same Kw expression.
- pH is a measure of acidity and is defined as -log[H3O+], with lower pH indicating higher acidity.
This document outlines the key objectives and concepts around acid-base equilibria, including:
- Defining strong and weak acids/bases using Bronsted-Lowry theory and discussing conjugate acid-base pairs
- Explaining the pH scale and relating pH, pOH, Ka, and pKa values
- Describing how to calculate the pH of strong acids/bases from their concentrations and vice versa
- Discussing how weak acids only partially dissociate in solution according to their acid dissociation constant (Ka)
- Demonstrating calculations for finding the pH of a solution of a weak acid using its Ka value
This document discusses acid-base equilibria and solubility equilibria. It covers the common ion effect and how it impacts equilibrium, buffer solutions, acid-base titrations and indicators, solubility equilibria including Ksp expressions and calculations, and the effects of pH and common ions on solubility. It also briefly mentions complex ion equilibria.
I hope You all like it. I hope It is very beneficial for you all. I really thought that you all get enough knowledge from this presentation. This presentation is about materials and their classifications. After you read this presentation you knowledge is not as before.
This document discusses acid-base equilibria and buffer solutions. It begins by explaining the common ion effect where adding a salt containing a common ion with a weak acid or base shifts the equilibrium towards the conjugate acid or base form. It then defines a buffer as a solution containing a weak acid or base along with its conjugate salt. The key properties of buffers are that they resist changes in pH. The Henderson-Hasselbalch equation relates the pH of a buffer solution to the ratio of concentrations of the conjugate base and acid. Examples are provided to show how to calculate the pH of buffer solutions and how buffers counteract additions of strong acids or bases.
The document discusses key concepts regarding acids and bases including: Bronsted-Lowery acids and bases, conjugate acid-base pairs, the pH scale, strong and weak acids and bases, acid-base properties of salts, and Lewis acids and bases. Key equations discussed include the ionization of water and the autoionization constant Kw. Sample problems are provided for calculating pH, percentage of ionization, and acid and base dissociation constants.
This document provides an overview of acids and bases including:
- Definitions of acids and bases according to Arrhenius, Brรธnsted-Lowry, and Lewis theories
- How acids and bases react in water, forming conjugates
- Factors that influence acid and base strength such as polarity, resonance, and electronegativity
- Calculations involving acid and base dissociation constants (Ka and Kb) to determine pH
L 10 alcohols-structure_nomenclature_classification_etc_pch217_2013_2014hmfb
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This document discusses alcohols, including their structure, nomenclature, classification, physical properties, acidity and basicity, and methods of preparation. Key points covered include that alcohols contain an -OH functional group, can be classified as primary, secondary or tertiary based on carbon atom bonding, associate through hydrogen bonding affecting physical properties, and can be prepared through fermentation, hydration of alkenes, nucleophilic substitution, and reduction of carbonyl compounds.
This document discusses acid-base titrations. It begins with an introduction to acid-base theories such as Arrhenius, Brรธnsted-Lowry, and Lewis theories. It then covers acid-base equilibria in water including the self-ionization of water and the pH scale. The document discusses several topics relevant to acid-base titrations including buffer solutions, indicators, and titration curves. It provides examples of calculating pH for different types of solutions including weak acids, salts, and buffers. The summary concludes with an overview of requirements for a successful acid-base titration.
In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C=O. It is common to several classes of organic compounds, as part of many larger functional groups. A compound containing a carbonyl group is often referred to as a carbonyl compound.
This document discusses key concepts regarding acid-base chemistry and carbonate equilibria. It defines strong acids and bases as those that fully dissociate in water. Acid and base strength is related to their dissociation constants, with higher K values indicating stronger acids and bases. Carbon dioxide forms carbonic acid in water, which exists in equilibrium with bicarbonate and carbonate ions. Bjerrum plots illustrate how pH controls the dominant carbon species. Buffering capacity is explained using the Henderson-Hasselbach equation. Carbonate speciation is derived for open systems in contact with the atmosphere and controlled by carbon dioxide fugacity.
The document discusses various properties of acids and bases, including that acids are sour and donate protons while bases are bitter and accept protons. It also discusses conjugate acid-base pairs, water's ability to act as an acid or base through self-ionization, and the pH scale. Key concepts covered include Brรธnsted-Lowry definitions of acids and bases, conjugate acid-base pairs, calculating pH and pOH, and neutralization reactions between acids and bases.
The document discusses acids, bases, and salt hydrolysis. Acids are substances that donate hydrogen ions in water, while bases donate hydroxide ions. The modified Arrhenius definition accounts for salts dissociating in water, with their ions sometimes accepting or donating hydrogen ions. This causes solutions of salts to be slightly acidic or basic, explaining why some neutralization reactions do not reach a pH of 7. Examples show sodium acetate hydrolyzing to produce hydroxide ions, making its solution basic, while ammonium chloride hydrolyzes to produce hydrogen ions, making its solution acidic.
The document discusses several topics related to medical chemistry including:
1) Hydrolysis of salts derived from weak acids/bases can cause solutions to be slightly acidic or alkaline as the ions undergo reactions with water to reach equilibrium concentrations based on acid/base dissociation constants.
2) Buffer solutions resist pH changes upon addition of small amounts of acid or base through equilibria involving both acidic and basic components of comparable concentrations.
3) Aqueous colloidal dispersions can be stabilized by electric charge alone or by charge and solvation shells, with solubility of hydrophilic particles depending on salt concentration and competition for hydration shells.
This document provides an overview of biochemistry concepts including macromolecules, biochemical processes, and the connection between structure and function at the molecular level. Key topics covered include proteins, enzymes, lipids, membranes and transport, carbohydrates, metabolism, nucleic acids, intermolecular forces, equilibrium, acid/base theory, and buffers. The document emphasizes that understanding biochemical functions requires knowledge of chemistry concepts like oxidation-reduction, thermodynamics, and organic reactions.
Analytics for http://forensicchemistry.lincoln.ac.uk, Feb/March 2011ulcerd
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The document summarizes website analytics for the forensicchemistry.lincoln.ac.uk site from February 20, 2011 to March 21, 2011. It received 45 visits from 11 countries over this period. The majority of traffic came from search engines (53.33%) and referring sites (37.78%). The United Kingdom contributed the most visits (14) and had the highest average pages per visit (2.14) and average time on site (1 minute, 44 seconds). The overall bounce rate was 64.44% and 93.33% of visits were from new visitors.
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This document summarizes webpage analytics for content from the Introductory Chemistry institutional repository from February 21 to March 21. It shows the number of pageviews and unique pageviews for each page, as well as average time on page, bounce rate, exit percentage, and cost index for the overall page and individual pages. The most visited page was /2366/ with 15 pageviews and 14 unique pageviews. The average time on page for all content was 53 seconds, with bounce and exit rates lower than the site average.
Organic Chemistry: Classification of Organic Compounds: Seminarulcerd
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This document discusses various organic functional groups including alcohols, aldehydes, ketones, carboxylic acids, esters, ethers, amines, amides, halogenoalkanes, nitriles, nitro compounds, and thiols. It provides examples of each functional group and discusses their classifications. Primary, secondary, and tertiary alcohols and amines are defined. Common illegal and recreational drugs like amphetamines, aspirin, cannabis, LSD, cocaine, morphine, and codeine are analyzed in terms of their functional group components.
1. The document discusses moles, molar mass, molarity, and provides example calculations involving these concepts. Molarity is defined as the number of moles of solute per liter of solution.
2. The document then provides 21 practice problems calculating things like the number of moles or grams of various substances, the molarity of different solutions, and multi-step dilution problems.
3. Students are asked to use the concepts of moles, molar mass, and molarity to solve quantitative chemistry problems involving substances in solutions.
Calculations using standard enthalpies of formationulcerd
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1. The document provides standard enthalpies of formation (ฮfHยฐ) for various compounds and asks the reader to use these values to calculate the enthalpy change for 10 chemical reactions and processes.
2. It lists the standard enthalpies of formation for common compounds such as water, carbon dioxide, benzene, cyclohexane, calcium carbonate, quicklime, sulfur dioxide, sulfuric acid, ethanol, bromoethane and more.
3. The reader is to apply Hess's law and add or subtract the given standard enthalpies of formation to determine the enthalpy change for the 10 processes listed, such as the enthalpy of solution of hydrogen bromide gas and
Organic Chemistry: Classification of Organic Compoundsulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Structure of Matter. Elements, Ions & Isotopes ulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Chemical Structure: Chemical Bonding. Polar Bondsulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
This document discusses various topics in thermochemistry including:
- Enthalpy changes in chemical reactions and how they are measured using calorimetry. Exothermic and endothermic reactions are explained.
- Hess's law, which states that the enthalpy change of a reaction is independent of the reaction pathway. It can be used to calculate enthalpy changes.
- Standard enthalpies of formation and how they allow calculation of enthalpy changes using Hess's law and bond dissociation enthalpies.
- Measuring enthalpy changes using bomb calorimetry and coffee cup calorimetry. Limitations of each method are discussed.
Chemical and Physical Properties: Radioactivity & Radioisotopes ulcerd
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Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
Lecture materials for the Introductory Chemistry course for Forensic Scientists, University of Lincoln, UK. See http://forensicchemistry.lincoln.ac.uk/ for more details.
โPencils and Pixelsโ is a learning resource aimed at helping you to improve your communication skills through drawing. An important part of the design process is to develop ideas from the imagination and share those ideas in the wider world. Whether you are having a conversation with yourself or with others, improving your drawing skills will help you to explain that most important of questions, โbut what will it look like?
For more information and related videos, visit: http://pencilsandpixels.blogs.lincoln.ac.uk/lessons/lesson-1/
โPencils and Pixelsโ is a learning resource aimed at helping you to improve your communication skills through drawing. An important part of the design process is to develop ideas from the imagination and share those ideas in the wider world. Whether you are having a conversation with yourself or with others, improving your drawing skills will help you to explain that most important of questions, โbut what will it look like?
For more information and related videos, visit: http://pencilsandpixels.blogs.lincoln.ac.uk/lessons/lesson-1/
This presentation was provided by Rebecca Benner, Ph.D., of the American Society of Anesthesiologists, for the second session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session Two: 'Expanding Pathways to Publishing Careers,' was held June 13, 2024.
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...TechSoup
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Whether you're new to SEO or looking to refine your existing strategies, this webinar will provide you with actionable insights and practical tips to elevate your nonprofit's online presence.
Chapter wise All Notes of First year Basic Civil Engineering.pptxDenish Jangid
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Chapter wise All Notes of First year Basic Civil Engineering
Syllabus
Chapter-1
Introduction to objective, scope and outcome the subject
Chapter 2
Introduction: Scope and Specialization of Civil Engineering, Role of civil Engineer in Society, Impact of infrastructural development on economy of country.
Chapter 3
Surveying: Object Principles & Types of Surveying; Site Plans, Plans & Maps; Scales & Unit of different Measurements.
Linear Measurements: Instruments used. Linear Measurement by Tape, Ranging out Survey Lines and overcoming Obstructions; Measurements on sloping ground; Tape corrections, conventional symbols. Angular Measurements: Instruments used; Introduction to Compass Surveying, Bearings and Longitude & Latitude of a Line, Introduction to total station.
Levelling: Instrument used Object of levelling, Methods of levelling in brief, and Contour maps.
Chapter 4
Buildings: Selection of site for Buildings, Layout of Building Plan, Types of buildings, Plinth area, carpet area, floor space index, Introduction to building byelaws, concept of sun light & ventilation. Components of Buildings & their functions, Basic concept of R.C.C., Introduction to types of foundation
Chapter 5
Transportation: Introduction to Transportation Engineering; Traffic and Road Safety: Types and Characteristics of Various Modes of Transportation; Various Road Traffic Signs, Causes of Accidents and Road Safety Measures.
Chapter 6
Environmental Engineering: Environmental Pollution, Environmental Acts and Regulations, Functional Concepts of Ecology, Basics of Species, Biodiversity, Ecosystem, Hydrological Cycle; Chemical Cycles: Carbon, Nitrogen & Phosphorus; Energy Flow in Ecosystems.
Water Pollution: Water Quality standards, Introduction to Treatment & Disposal of Waste Water. Reuse and Saving of Water, Rain Water Harvesting. Solid Waste Management: Classification of Solid Waste, Collection, Transportation and Disposal of Solid. Recycling of Solid Waste: Energy Recovery, Sanitary Landfill, On-Site Sanitation. Air & Noise Pollution: Primary and Secondary air pollutants, Harmful effects of Air Pollution, Control of Air Pollution. . Noise Pollution Harmful Effects of noise pollution, control of noise pollution, Global warming & Climate Change, Ozone depletion, Greenhouse effect
Text Books:
1. Palancharmy, Basic Civil Engineering, McGraw Hill publishers.
2. Satheesh Gopi, Basic Civil Engineering, Pearson Publishers.
3. Ketki Rangwala Dalal, Essentials of Civil Engineering, Charotar Publishing House.
4. BCP, Surveying volume 1
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the bodyโs response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
1. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Reversible Reactions and Chemical Equilibrium University of Lincoln presentation
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11. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Units of K c Solution A Now try for solutions B and C
12. Acids and Bases This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
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22. pK a values (data tables) This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Acid pK a Conjugate base H 3 PO 4 2.12 H 2 PO 4 - HNO 2 3.34 NO 2 - H 2 CO 3 6.37 HCO 3 - HCN 9.31 CN - HCO 3 - 10.25 CO 3 2-
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24. Henderson-Hasselbach This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License For weak acids Use the equation with the example in the previous slide. Do you come to the same conclusion regarding the ratio of un-ionised to ionised acid molecules?
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26. Henderson-Hasselbach This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License For weak bases Use the equation with the example in the previous slide. Do you come to the same conclusion regarding the ratio of un-ionised to ionised acid molecules?
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34. Buffers This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License
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37. Buffers This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Henderson-Hasselbach equation Acidic buffers
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40. An alkaline buffer: ammonia solution and ammonium chloride This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 2.0 UK: England & Wales License Note the base/salt ratio What is the pH of a buffer with base:salt ratio = 1? Calculate the base:salt ratios for pH 8.5 and pH 10.5
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Editor's Notes
Strong acids dissociate completely in water. Concentrated acids contain several moles of substance per dm3.
When an acid dissociated, the H+ ions actually combine with H2O to produce H30+ (oxonium ions, or hydroxonium ions). H+ + H2O ๏ฎ H3O+ A- is referred to as the conjugate base of the acid; I.e.the ions associated with the acid and capable of recombining with the H+ ion. More on this later. E.g. Ka values HCl = 7.2 x 10 10 acetic acid = 1.8 x 10-5
Water can dissociate:I.e. separate into its ionic components. This dissociation is very partial, in fact one water molecule in 550 million is ionised at any given moment. Because of this to all intents and purposes the concentration of water is taken to be constant
Kw is really Keq x another constant for H2O.
Hopefully you have all used at some point universal pH paper green = 7 blue = very alkaline red = very acidic
0.1M HNO3 is fully ionised: HNO3 ๏ฎ H+ + NO3- thus, have 0.1moles in 1dm3 of H+ ions. Thus put 0.1 into equation to give a pH equalling 1. CH3COOH is partially ionised: CH3COOH ๏ซ CH3C00- + H+ only have 0.001 or 10-3 moles of H+ ions, thus pH = 3. A pH meter musing a H electrode to measure the pH of a solution.
0.1M NaOH - strong alkali-completely ionised NaOH ๏ฎ Na + + OH- Thus, 0.1M NaOH contains 0.1M of OH- ions in 1 dm3. Put into equation. 10-13 which gives a pH = 13.
Used in the lab: reagents can be added to solutions without pH altering and reactions carried out. Absorption of CO2 and lab fumes may also the pH of a solution. 15.7 โ Housecroft โ P462 - 467 Making use of the partial dissociation of weak acids and bases