This slide is on chloroform - it's preparation, occurrence, properties, history & uses. This slide is school friendly means you can use it for your school project.
Ethyl chloride is a colorless, flammable gas or refrigerated liquid with a faintly sweet odor. Its chemical formula is C2H5Cl. It should be stored in a cool place below 120°F and away from fire or flames. Ethyl chloride is produced through the hydrochlorination of ethylene and was formerly used as a refrigerant, aerosol propellant, and anesthetic. Its only major current use is in treating cellulose to make ethylcellulose.
Chloroform is a colorless, sweet-smelling liquid that is produced commercially by heating a mixture of chlorine and chloromethane or methane. It has a variety of uses including as a solvent in the pharmaceutical industry, for producing dyes and pesticides, and as a refrigerant. Historically it was used as a surgical anesthetic but has been replaced by safer drugs. Chloroform is considered hazardous due to its toxicity if inhaled or ingested, and prolonged exposure may cause health issues like kidney and liver damage.
THIS SLIDE CONTAIN ABOUT QUALITATIVE TEST, STRUCTURE AND USES OF DIFFERENT CARBONYL COMPOUNDS LIKE FORMALDEHYDE, PARALDEHYDE, ACETONE, CHLORAL HYDRATE, HEXAMINE, BENZALDEHYDE, VANILIN AND CINNAMALDEHYDE
B.Pharm I Year II Sem. SN1 and SN2 reactions, kinetics, order of reactivity of alkyl halides, stereochemistry and rearrangement of carbocations.
SN1 versus SN2 reactions, Factors affecting SN1 and SN2 reactions.
Structure and uses of ethylchloride, Chloroform, trichloroethylene, tetrachloroethylene,
dichloromethane, tetrachloromethane and iodoform.
Alcohols, Qualitative tests for Alcohol, Structure and uses of Ethyl alcohol, chlorobutanol, Cetosterylalcohol, Benzyl alcohol, Glycerol, Propylene glycol
This document provides information about carbonyl compounds, specifically aldehydes and ketones. It discusses their IUPAC nomenclature, methods of preparation including oxidation of alcohols and oxidative cleavage of alkenes, and physical and chemical properties. The chemical reactions covered include nucleophilic addition, reduction, condensation, and oxidation reactions. Examples of important aldehydes and ketones are also mentioned along with their structures and uses.
Ethyl chloride is a colorless, flammable gas or refrigerated liquid with a faintly sweet odor. Its chemical formula is C2H5Cl. It should be stored in a cool place below 120°F and away from fire or flames. Ethyl chloride is produced through the hydrochlorination of ethylene and was formerly used as a refrigerant, aerosol propellant, and anesthetic. Its only major current use is in treating cellulose to make ethylcellulose.
Chloroform is a colorless, sweet-smelling liquid that is produced commercially by heating a mixture of chlorine and chloromethane or methane. It has a variety of uses including as a solvent in the pharmaceutical industry, for producing dyes and pesticides, and as a refrigerant. Historically it was used as a surgical anesthetic but has been replaced by safer drugs. Chloroform is considered hazardous due to its toxicity if inhaled or ingested, and prolonged exposure may cause health issues like kidney and liver damage.
THIS SLIDE CONTAIN ABOUT QUALITATIVE TEST, STRUCTURE AND USES OF DIFFERENT CARBONYL COMPOUNDS LIKE FORMALDEHYDE, PARALDEHYDE, ACETONE, CHLORAL HYDRATE, HEXAMINE, BENZALDEHYDE, VANILIN AND CINNAMALDEHYDE
B.Pharm I Year II Sem. SN1 and SN2 reactions, kinetics, order of reactivity of alkyl halides, stereochemistry and rearrangement of carbocations.
SN1 versus SN2 reactions, Factors affecting SN1 and SN2 reactions.
Structure and uses of ethylchloride, Chloroform, trichloroethylene, tetrachloroethylene,
dichloromethane, tetrachloromethane and iodoform.
Alcohols, Qualitative tests for Alcohol, Structure and uses of Ethyl alcohol, chlorobutanol, Cetosterylalcohol, Benzyl alcohol, Glycerol, Propylene glycol
This document provides information about carbonyl compounds, specifically aldehydes and ketones. It discusses their IUPAC nomenclature, methods of preparation including oxidation of alcohols and oxidative cleavage of alkenes, and physical and chemical properties. The chemical reactions covered include nucleophilic addition, reduction, condensation, and oxidation reactions. Examples of important aldehydes and ketones are also mentioned along with their structures and uses.
Chloroethane is used as an anesthetic, refrigerant, aerosol propellant, and blowing agent for foam packaging. It is also used to diagnose dead teeth by placing it on suspect teeth - if the tooth is dead, it will not respond to the chloroethane. Chloroethane was historically used to produce tetraethyllead as an anti-knock additive for gasoline. It is not considered carcinogenic but high concentrations starting at 9-12% can be toxic, affecting heart rate.
Preparation, reactions, Acidity, effect of substituents on acidity, structure and uses of carboxylic acid and identification tests for carboxylic acid, amide and ester
The document discusses elimination reactions, specifically E1 and β-elimination reactions. It explains that E1 reactions proceed through a two-step unimolecular mechanism, with the first step being rate-determining. Factors that affect E1 reactions include the stability of the carbocation intermediate, steric effects, and the ability of the base to stabilize the carbocation. Rearrangements can also occur through carbocation migration to form more stable products.
Tetra substituted alkenes are the most stable, followed by tri, di, and mono substituted alkenes. Within di-substituted alkenes, the trans isomer is more stable than the cis isomer due to less steric hindrance. The degree of stability is directly proportional to the amount of conjugation and substitution on the alkene. Heat of hydrogenation can be used to determine the relative stability and energy of alkene isomers, with less stable isomers requiring more energy for hydrogenation. For example, cis-2-butene requires more energy than trans-2-butene during hydrogenation.
The document discusses various tests to identify primary, secondary, and tertiary amines. It describes the solubility test, litmus test, carbylamine test, nitrous acid test, azo-dye test, and Hinsberg test. The solubility test checks if a compound dissolves in mineral acid, indicating it may be an amine. The litmus test checks if a compound turns red litmus blue, showing it is basic. The carbylamine, nitrous acid, and azo-dye tests identify primary, secondary, and tertiary amines based on their reactions. The Hinsberg test uses precipitation and solubility patterns to distinguish between the three amine types.
This document discusses the acidity of carboxylic acids. It explains that in an aqueous solution, carboxylic acid molecules interact with water molecules to form carboxylate ions and hydronium ions. The acidity constant (Ka) is a measure of a carboxylic acid's acidity, with a higher Ka value indicating a stronger acid. Common carboxylic acids like acetic acid have a lower Ka than strong acids like hydrochloric acid, making them weaker acids that are only partially ionized in water. Substituents on carboxylic acids can affect their acidity.
Classification, Nomenclature and structural isomerism of organic compound Ganesh Mote
Classification of organic compound, Nomenclature of alkane, alkene, alkyne, alcohol, alkyl halide, aldehyde, ketone, carboxylic acid and its derivatives, amines, ethers, polyfunctional groups and structural isomerism of organic compounds
The aldol condensation reaction allows carbonyl compounds containing an α-hydrogen atom to undergo condensation. It is a reversible reaction that proceeds through an enolate intermediate formed when hydroxide deprotonates the α-hydrogen. The enolate then acts as a nucleophile that attacks the electrophilic carbonyl carbon of an aldehyde or ketone. Protonation of the resulting alkoxide forms the β-hydroxy aldehyde or ketone product. The reaction can join two different aldehydes or ketones in a crossed-aldol condensation that expands the synthetic possibilities.
The aldol condensation reaction involves the reaction of two carbonyl compounds in the presence of a strong base to form a β-hydroxyaldehyde or β-hydroxyketone. The reaction proceeds through the formation of an enolate ion intermediate that acts as a nucleophile, attacking the carbonyl carbon of the other molecule. This forms a carbon-carbon bond between the α-carbon of the donor molecule and the carbonyl carbon of the acceptor molecule. The aldol condensation reaction is useful for synthesizing larger molecules from simple starting materials and plays an important role in biochemical processes such as gluconeogenesis.
nucleophilic addition reaction sem ii poc iAtulBendale2
This document discusses nucleophilic addition reactions to carbonyl compounds. It defines nucleophiles as electron rich species that donate electron pairs to form bonds. Strong nucleophiles like hydroxide are discussed along with examples of nucleophilic addition including addition of water, alcohols, hydrogen cyanide, organometallic reagents, and ammonia derivatives to carbonyl groups. The mechanism of nucleophilic addition is described as the nucleophile attacking the carbonyl carbon to form a tetrahedral intermediate that then collapses to form the alcohol, hydrate, imine or other product.
The Cannizzaro reaction is a disproportionation reaction discovered by Italian chemist Stanislao Cannizzaro in 1853. In the reaction, an aldehyde without an alpha hydrogen undergoes a base-catalyzed reaction in the presence of a strong base like potassium hydroxide or sodium hydroxide and heat to produce an alcohol and a carboxylic acid as products. The reaction allows for the conversion of aldehydes into mixtures of carboxylic acids and alcohols.
The combination of a carbonyl group and a hydroxyl on the same carbon atom is called a carboxyl group. Compounds containing the carboxyl group are called carboxylic acids. The carboxyl group is one of the most widely occurring functional groups in organic chemistry.
Aromatic Carboxylic acids: Carboxylic acids have an aryl group bound to the carboxyl group is known as aromatic carboxylic acids. The general formula of an aliphatic aromatic carboxylic acid is Ar-COOH.
Acidity of carboxylic acid:
A carboxylic acid may dissociate in water to give a proton and a carboxylate ion. Dissociation of a carboxylic acid involves breaking an O-H bond gives a carboxylate ion with the negative charge spread out equally over two oxygen atoms, compared with just one oxygen atom in an alkoxide ion. The delocalized charge makes the carboxylate ion more stable therefore; dissociation of a carboxylic acid to a carboxylate ion is less endothermic.
Preparation Methods:
1. Oxidation:
The oxidation of aldehyde with oxidizing agents such as CrO3 to forms carboxylic acids containing the same numbers of carbon atoms with a oxidizing agents like chromic acid, chromium trioxide. The silver oxide (Ag2O) in aqueous ammonia solution (Tollen’s reagent) is mild reagent give good yield at room temperature. E.g. Acetaldehyde reacts with CrO3 in aqueous acid to give acetic acid.
2. Grignard reagents (from CO2):
Carboxylic acid can be prepared by the reaction of Grignard reagent (alkyl magnesium halide) with carbon dioxide (CO2) in presence of dry ether. Grignard reagents react with carbon dioxide to forms a magnesium carboxylates which on hydrolysis by dilute HCl produces carboxylic acids.
3. Hydrolysis of nitrile:
The hydrolysis of nitrile or cyanide in presence of dilute acid to forms a carboxylic acid. In this reaction –CN group is converted to a –COOH group.
4. Hydrolysis Reactions:
All the carboxylic acid derivatives can be hydrolyzed into the carboxylic acid in the acidic or basic media; the hydrolysis reaction is fast and occurs in presence of water with no acid or base catalyst.
1. From Ester (Hydrolysis of ester): Ester can be hydrolyzed in either acidic or basic medium to yield carboxylic acid. The ester is heated with an excess of water contains strong acid or base catalyst.
Properties of Carboxylic Acids:
1. Low molecular weights carboxylic acids are colourless liquid at room temperature i.e. lower member ate liquid up to C9 and have characteristic odors whereas higher members are solid.
2. Carboxylic acids are polar organic compound. Low molecular weight carboxylic acids (first four members) are soluble in water whereas solubility in water decrease as molecular weight and chain lengthing increases.
3. Aromatic acids are insoluble in water.
4. Carboxylic acids have higher melting and boiling point due to their capacity to readily form stable hydrogen-bonded dimers.
The document discusses carbocations, which are carbon-containing molecules with a positive charge. It defines different types of carbocations based on the groups attached to the charged carbon atom, such as primary, secondary, tertiary, allylic, benzylic, vinyl, and phenyl carbocations. The document also discusses the structure, stability, and rearrangement of carbocations. Carbocations can rearrange into more stable configurations by shifting bonds to form secondary or tertiary carbocations. The stability of carbocations is affected by the number of carbon groups attached, neighboring electron-withdrawing groups, and hybridization of the charged carbon atom.
Structure, application and uses ddt, saccharin, bhc and chloramine copyMayankKumarSaini1
This document provides information on the structures, applications, and uses of DDT, BHC, saccharin, and chloramine. It discusses:
1) The chemical structures of DDT, BHC, saccharin, and chloramine. DDT and BHC are organochlorine compounds while saccharin is a cyclic sulfimide. Chloramines refer to derivatives of ammonia and organic amines.
2) The uses of these compounds as insecticides and pharmaceutical treatments. DDT was widely used to combat malaria and typhus. BHC is used as an agricultural insecticide and to treat lice and scabies. Saccharin is used as an artificial sweetener.
Chlorine is the most abundant member of the halogen family of periodic table elements. Chlorine is an important chemical in our day-to-day life. Chlorine is a clear amber-colored liquid about 1.5 times heavier than water.
The document discusses several organic compounds including chloroform, ethyl alcohol, and acetone. It provides detailed information on the properties, production methods, reactions, and uses of chloroform and ethyl alcohol. For chloroform, it describes its molecular structure, history of discovery, industrial production through heating chlorine with methane, and past and current uses such as an anesthetic and refrigerant. For ethyl alcohol, it outlines its chemical structure, production through fermentation of sugars by yeast as well as from ethylene, common reactions like ester formation, and its flammability.
Chloroethane is used as an anesthetic, refrigerant, aerosol propellant, and blowing agent for foam packaging. It is also used to diagnose dead teeth by placing it on suspect teeth - if the tooth is dead, it will not respond to the chloroethane. Chloroethane was historically used to produce tetraethyllead as an anti-knock additive for gasoline. It is not considered carcinogenic but high concentrations starting at 9-12% can be toxic, affecting heart rate.
Preparation, reactions, Acidity, effect of substituents on acidity, structure and uses of carboxylic acid and identification tests for carboxylic acid, amide and ester
The document discusses elimination reactions, specifically E1 and β-elimination reactions. It explains that E1 reactions proceed through a two-step unimolecular mechanism, with the first step being rate-determining. Factors that affect E1 reactions include the stability of the carbocation intermediate, steric effects, and the ability of the base to stabilize the carbocation. Rearrangements can also occur through carbocation migration to form more stable products.
Tetra substituted alkenes are the most stable, followed by tri, di, and mono substituted alkenes. Within di-substituted alkenes, the trans isomer is more stable than the cis isomer due to less steric hindrance. The degree of stability is directly proportional to the amount of conjugation and substitution on the alkene. Heat of hydrogenation can be used to determine the relative stability and energy of alkene isomers, with less stable isomers requiring more energy for hydrogenation. For example, cis-2-butene requires more energy than trans-2-butene during hydrogenation.
The document discusses various tests to identify primary, secondary, and tertiary amines. It describes the solubility test, litmus test, carbylamine test, nitrous acid test, azo-dye test, and Hinsberg test. The solubility test checks if a compound dissolves in mineral acid, indicating it may be an amine. The litmus test checks if a compound turns red litmus blue, showing it is basic. The carbylamine, nitrous acid, and azo-dye tests identify primary, secondary, and tertiary amines based on their reactions. The Hinsberg test uses precipitation and solubility patterns to distinguish between the three amine types.
This document discusses the acidity of carboxylic acids. It explains that in an aqueous solution, carboxylic acid molecules interact with water molecules to form carboxylate ions and hydronium ions. The acidity constant (Ka) is a measure of a carboxylic acid's acidity, with a higher Ka value indicating a stronger acid. Common carboxylic acids like acetic acid have a lower Ka than strong acids like hydrochloric acid, making them weaker acids that are only partially ionized in water. Substituents on carboxylic acids can affect their acidity.
Classification, Nomenclature and structural isomerism of organic compound Ganesh Mote
Classification of organic compound, Nomenclature of alkane, alkene, alkyne, alcohol, alkyl halide, aldehyde, ketone, carboxylic acid and its derivatives, amines, ethers, polyfunctional groups and structural isomerism of organic compounds
The aldol condensation reaction allows carbonyl compounds containing an α-hydrogen atom to undergo condensation. It is a reversible reaction that proceeds through an enolate intermediate formed when hydroxide deprotonates the α-hydrogen. The enolate then acts as a nucleophile that attacks the electrophilic carbonyl carbon of an aldehyde or ketone. Protonation of the resulting alkoxide forms the β-hydroxy aldehyde or ketone product. The reaction can join two different aldehydes or ketones in a crossed-aldol condensation that expands the synthetic possibilities.
The aldol condensation reaction involves the reaction of two carbonyl compounds in the presence of a strong base to form a β-hydroxyaldehyde or β-hydroxyketone. The reaction proceeds through the formation of an enolate ion intermediate that acts as a nucleophile, attacking the carbonyl carbon of the other molecule. This forms a carbon-carbon bond between the α-carbon of the donor molecule and the carbonyl carbon of the acceptor molecule. The aldol condensation reaction is useful for synthesizing larger molecules from simple starting materials and plays an important role in biochemical processes such as gluconeogenesis.
nucleophilic addition reaction sem ii poc iAtulBendale2
This document discusses nucleophilic addition reactions to carbonyl compounds. It defines nucleophiles as electron rich species that donate electron pairs to form bonds. Strong nucleophiles like hydroxide are discussed along with examples of nucleophilic addition including addition of water, alcohols, hydrogen cyanide, organometallic reagents, and ammonia derivatives to carbonyl groups. The mechanism of nucleophilic addition is described as the nucleophile attacking the carbonyl carbon to form a tetrahedral intermediate that then collapses to form the alcohol, hydrate, imine or other product.
The Cannizzaro reaction is a disproportionation reaction discovered by Italian chemist Stanislao Cannizzaro in 1853. In the reaction, an aldehyde without an alpha hydrogen undergoes a base-catalyzed reaction in the presence of a strong base like potassium hydroxide or sodium hydroxide and heat to produce an alcohol and a carboxylic acid as products. The reaction allows for the conversion of aldehydes into mixtures of carboxylic acids and alcohols.
The combination of a carbonyl group and a hydroxyl on the same carbon atom is called a carboxyl group. Compounds containing the carboxyl group are called carboxylic acids. The carboxyl group is one of the most widely occurring functional groups in organic chemistry.
Aromatic Carboxylic acids: Carboxylic acids have an aryl group bound to the carboxyl group is known as aromatic carboxylic acids. The general formula of an aliphatic aromatic carboxylic acid is Ar-COOH.
Acidity of carboxylic acid:
A carboxylic acid may dissociate in water to give a proton and a carboxylate ion. Dissociation of a carboxylic acid involves breaking an O-H bond gives a carboxylate ion with the negative charge spread out equally over two oxygen atoms, compared with just one oxygen atom in an alkoxide ion. The delocalized charge makes the carboxylate ion more stable therefore; dissociation of a carboxylic acid to a carboxylate ion is less endothermic.
Preparation Methods:
1. Oxidation:
The oxidation of aldehyde with oxidizing agents such as CrO3 to forms carboxylic acids containing the same numbers of carbon atoms with a oxidizing agents like chromic acid, chromium trioxide. The silver oxide (Ag2O) in aqueous ammonia solution (Tollen’s reagent) is mild reagent give good yield at room temperature. E.g. Acetaldehyde reacts with CrO3 in aqueous acid to give acetic acid.
2. Grignard reagents (from CO2):
Carboxylic acid can be prepared by the reaction of Grignard reagent (alkyl magnesium halide) with carbon dioxide (CO2) in presence of dry ether. Grignard reagents react with carbon dioxide to forms a magnesium carboxylates which on hydrolysis by dilute HCl produces carboxylic acids.
3. Hydrolysis of nitrile:
The hydrolysis of nitrile or cyanide in presence of dilute acid to forms a carboxylic acid. In this reaction –CN group is converted to a –COOH group.
4. Hydrolysis Reactions:
All the carboxylic acid derivatives can be hydrolyzed into the carboxylic acid in the acidic or basic media; the hydrolysis reaction is fast and occurs in presence of water with no acid or base catalyst.
1. From Ester (Hydrolysis of ester): Ester can be hydrolyzed in either acidic or basic medium to yield carboxylic acid. The ester is heated with an excess of water contains strong acid or base catalyst.
Properties of Carboxylic Acids:
1. Low molecular weights carboxylic acids are colourless liquid at room temperature i.e. lower member ate liquid up to C9 and have characteristic odors whereas higher members are solid.
2. Carboxylic acids are polar organic compound. Low molecular weight carboxylic acids (first four members) are soluble in water whereas solubility in water decrease as molecular weight and chain lengthing increases.
3. Aromatic acids are insoluble in water.
4. Carboxylic acids have higher melting and boiling point due to their capacity to readily form stable hydrogen-bonded dimers.
The document discusses carbocations, which are carbon-containing molecules with a positive charge. It defines different types of carbocations based on the groups attached to the charged carbon atom, such as primary, secondary, tertiary, allylic, benzylic, vinyl, and phenyl carbocations. The document also discusses the structure, stability, and rearrangement of carbocations. Carbocations can rearrange into more stable configurations by shifting bonds to form secondary or tertiary carbocations. The stability of carbocations is affected by the number of carbon groups attached, neighboring electron-withdrawing groups, and hybridization of the charged carbon atom.
Structure, application and uses ddt, saccharin, bhc and chloramine copyMayankKumarSaini1
This document provides information on the structures, applications, and uses of DDT, BHC, saccharin, and chloramine. It discusses:
1) The chemical structures of DDT, BHC, saccharin, and chloramine. DDT and BHC are organochlorine compounds while saccharin is a cyclic sulfimide. Chloramines refer to derivatives of ammonia and organic amines.
2) The uses of these compounds as insecticides and pharmaceutical treatments. DDT was widely used to combat malaria and typhus. BHC is used as an agricultural insecticide and to treat lice and scabies. Saccharin is used as an artificial sweetener.
Chlorine is the most abundant member of the halogen family of periodic table elements. Chlorine is an important chemical in our day-to-day life. Chlorine is a clear amber-colored liquid about 1.5 times heavier than water.
The document discusses several organic compounds including chloroform, ethyl alcohol, and acetone. It provides detailed information on the properties, production methods, reactions, and uses of chloroform and ethyl alcohol. For chloroform, it describes its molecular structure, history of discovery, industrial production through heating chlorine with methane, and past and current uses such as an anesthetic and refrigerant. For ethyl alcohol, it outlines its chemical structure, production through fermentation of sugars by yeast as well as from ethylene, common reactions like ester formation, and its flammability.
This document discusses the members of the Halogen Jupiter group: Mahbooba moushumi Khan, Mahmudul islamsalmani, Shadman Shakib, and Abdullah Al Noman. It then provides information about the halogen elements fluorine, chlorine, bromine, iodine, and astatine including their discovery, physical and chemical properties, uses, and potential health effects.
This document summarizes information about various alkyl halides. It discusses the chemical structures, properties and uses of ethyl chloride, chloroform, tetrachloroethylene, trichloroethylene, tetrachloromethane, dichloromethane and iodoform. Many of these compounds are or were used as solvents, refrigerants, degreasers, paint strippers, dry cleaning fluids and disinfectants due to their volatility and ability to dissolve organic materials.
Chlorine is effective as both a sanitizer and oxidizer in pools. As a sanitizer, chlorine kills bacteria and microorganisms. As an oxidizer, it chemically breaks down and removes contaminants from the water. The primary sanitizing agent resulting from chlorine products is hypochlorous acid. Hypochlorous acid exists in equilibrium with hypochlorite ions, and the ratio depends on pH. At a pH of 7.5 the ratio is equal, favoring HOCl at lower pH and OCl- at higher pH. Hypochlorous acid is the most effective form of chlorine sanitizer. Stabilized chlorine products contain isocyanurates that bond chlorine
Full power point presentation for Alcohol, Phenol and Ethers.
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Anyone can prefer to my ppt.
Hope every one will like it and support for making more for all.
The document summarizes an experiment investigating the effect of light intensity on the amount of chlorophyll in the plant species Cicer arietinum. Seeds were divided into 7 groups and placed in locations with varying light intensities ranging from 0 to 1200 lux. After 3 weeks, plant length, biomass, and chlorophyll content were measured. Chlorophyll content was determined through ethanol extraction and titration. The results showed that plants exposed to lower light intensities were longer with less chlorophyll, while higher light intensities produced shorter plants with more chlorophyll, until intensities exceeded 1200 lux. The study supported the hypothesis that chlorophyll amount increases with light intensity up to a point, after which destruction exceeds formation.
Ozone is a powerful disinfectant that is more effective than chlorine at killing microorganisms in swimming pools. It also eliminates chloramines that cause unpleasant odors and irritation. Using ozone improves water clarity and reduces health risks from chlorine byproducts. The document discusses the benefits of ozone over chlorine for swimming pool water treatment and disinfection.
This document discusses water chlorination. It begins with an introduction to chlorination, explaining that it is a process used to kill bacteria, viruses, and other microbes in water. Section two discusses the history of chlorination, including its discovery and first uses. Section three explains the process of chlorinating water through shock chlorination. Section four covers the biochemistry of chlorine and how it kills pathogens. Section five notes some potential drawbacks, such as the production of disinfection byproducts. The final section describes how to chlorinate water at home through following CDC guidelines.
This document discusses disinfection and chlorination of water. It describes different disinfection methods like chlorination, ozonization, and UV rays. Chlorination involves adding small doses of chlorine or chlorine compounds to water to kill bacteria. The document discusses chlorine dosage, factors affecting chlorination, and special chlorination methods like pre-chlorination, double chlorination, and break point chlorination which involves adding chlorine until all organic matter is oxidized leaving residual chlorine.
Chemical disinfection of water involves using chlorine or other disinfectants like ozone gas or UV light to eliminate bacterial impurities. Chlorine is the most widely used disinfectant, either as gas, bleaching powder, or chloramines formed by mixing chlorine with ammonia. The document discusses the properties and methods of chlorine disinfection, including pre-chlorination before treatment, post-chlorination after filtration, and super-chlorination to destroy resistant organisms during epidemics. Effective disinfection requires maintaining chlorine residuals of 0.2-0.8 ppm for at least 30 minutes of contact time.
Chloromethanes namely methyl chloride (CH3Cl), methylene chloride (CH2Cl2), Chloroform (CHCl3) and Carbon Tetrachloride (CCl4) are produced by direct chlorination of Cl2 in a gas phase reaction without any catalyst.
This document provides information on various heterocyclic compounds. It discusses the definition and importance of heterocyclic chemistry. It then summarizes the structure, properties, synthesis, reactions and applications of several important 5-membered and 6-membered heterocyclic compounds that contain one or two heteroatoms such as oxygen, nitrogen, sulfur. These include furan, pyrrole, thiophene, pyridine, pyrimidine, quinoline, isoquinoline, indole, pyrazine, and pyrazole.
The document discusses the haloform reaction, where haloforms such as chloroform, bromoform, iodoform, and fluoroform are produced from methyl ketones or aldehydes in the presence of a base. It then describes each type of haloform reaction, providing the key details of their discovery, structures, and common uses. Iodoform and chloroform reactions were among the first discovered and have various medical and industrial applications. Bromoform and fluoroform are now mainly used as laboratory reagents.
Organic solutes enter water sources through human activity like improper disposal of volatile organic compounds. Alcohols, carboxylic acids, amines, and esters are usually soluble in water, while solubility decreases with longer carbon chain length. Common organic solutes include pesticides, gasoline components, and dry cleaning solvents. Though used in industry and agriculture, many organic solutes are toxic and can bioaccumulate, posing threats to life if released untreated into the environment. Strict handling and disposal is needed to reduce harm.
Solvents & their impact on environmentWishal Butt
A solvent is a substance that dissolves a solute resulting in a solution.
most of the solvents are combustible, often highly volatile and extremely flammable and they should always be handled with care.
An organic solvent containing oxygen as part of the molecular structure.
EXAMPLE:-
alcohols, glycol ethers, ketones, esters, and glycol ether.
USES
These solvents are widely used in paints, inks, pharmaceuticals, perfumes, adhesives, cosmetics, detergents, and food processing.During the synthesis of such solvents like alcohol, the residue of molasses is disposed off out of the industry containing microbes, may contaminate the soil & water.
Alcohol poisoning
Respiratory depressions
Low rate of metabolism by abnormal liver.
Disinfection chlorination chlorination derived by productssoumyatk
The document discusses sewage disinfection and the wastewater treatment process. It explains that the goal of wastewater treatment is to provide water free from pathogens, but primary, secondary, and tertiary treatment cannot remove 100% of waste and pathogens. Disinfection is needed to destroy remaining pathogens. The two main disinfection methods are physical (e.g. heating) and chemical (e.g. chlorination, ozonation). Chlorine is widely used for disinfection due to its availability, low cost, and ability to provide residuals that protect distribution systems. However, chlorine reactions can form harmful byproducts like trihalomethanes. Factors like water quality, temperature, pH, and contact time
This document summarizes information about triiodomethane and carbon tetrachloride. It discusses that triiodomethane was formerly used as an antiseptic but has been replaced due to its unpleasant odor. Carbon tetrachloride is produced for use in refrigerants, propellants, and solvents, though it poses health risks like liver damage and cancer. The document warns that carbon tetrachloride exposure can cause dizziness, nausea, and irregular heartbeats, and that it depletes the ozone layer when released into the air.
Similar to Chloroform - Formula, Preparation, Properties, Uses, History & Facts (20)
EWOCS-I: The catalog of X-ray sources in Westerlund 1 from the Extended Weste...Sérgio Sacani
Context. With a mass exceeding several 104 M⊙ and a rich and dense population of massive stars, supermassive young star clusters
represent the most massive star-forming environment that is dominated by the feedback from massive stars and gravitational interactions
among stars.
Aims. In this paper we present the Extended Westerlund 1 and 2 Open Clusters Survey (EWOCS) project, which aims to investigate
the influence of the starburst environment on the formation of stars and planets, and on the evolution of both low and high mass stars.
The primary targets of this project are Westerlund 1 and 2, the closest supermassive star clusters to the Sun.
Methods. The project is based primarily on recent observations conducted with the Chandra and JWST observatories. Specifically,
the Chandra survey of Westerlund 1 consists of 36 new ACIS-I observations, nearly co-pointed, for a total exposure time of 1 Msec.
Additionally, we included 8 archival Chandra/ACIS-S observations. This paper presents the resulting catalog of X-ray sources within
and around Westerlund 1. Sources were detected by combining various existing methods, and photon extraction and source validation
were carried out using the ACIS-Extract software.
Results. The EWOCS X-ray catalog comprises 5963 validated sources out of the 9420 initially provided to ACIS-Extract, reaching a
photon flux threshold of approximately 2 × 10−8 photons cm−2
s
−1
. The X-ray sources exhibit a highly concentrated spatial distribution,
with 1075 sources located within the central 1 arcmin. We have successfully detected X-ray emissions from 126 out of the 166 known
massive stars of the cluster, and we have collected over 71 000 photons from the magnetar CXO J164710.20-455217.
Mending Clothing to Support Sustainable Fashion_CIMaR 2024.pdfSelcen Ozturkcan
Ozturkcan, S., Berndt, A., & Angelakis, A. (2024). Mending clothing to support sustainable fashion. Presented at the 31st Annual Conference by the Consortium for International Marketing Research (CIMaR), 10-13 Jun 2024, University of Gävle, Sweden.
The technology uses reclaimed CO₂ as the dyeing medium in a closed loop process. When pressurized, CO₂ becomes supercritical (SC-CO₂). In this state CO₂ has a very high solvent power, allowing the dye to dissolve easily.
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
Immersive Learning That Works: Research Grounding and Paths ForwardLeonel Morgado
We will metaverse into the essence of immersive learning, into its three dimensions and conceptual models. This approach encompasses elements from teaching methodologies to social involvement, through organizational concerns and technologies. Challenging the perception of learning as knowledge transfer, we introduce a 'Uses, Practices & Strategies' model operationalized by the 'Immersive Learning Brain' and ‘Immersion Cube’ frameworks. This approach offers a comprehensive guide through the intricacies of immersive educational experiences and spotlighting research frontiers, along the immersion dimensions of system, narrative, and agency. Our discourse extends to stakeholders beyond the academic sphere, addressing the interests of technologists, instructional designers, and policymakers. We span various contexts, from formal education to organizational transformation to the new horizon of an AI-pervasive society. This keynote aims to unite the iLRN community in a collaborative journey towards a future where immersive learning research and practice coalesce, paving the way for innovative educational research and practice landscapes.
The binding of cosmological structures by massless topological defectsSérgio Sacani
Assuming spherical symmetry and weak field, it is shown that if one solves the Poisson equation or the Einstein field
equations sourced by a topological defect, i.e. a singularity of a very specific form, the result is a localized gravitational
field capable of driving flat rotation (i.e. Keplerian circular orbits at a constant speed for all radii) of test masses on a thin
spherical shell without any underlying mass. Moreover, a large-scale structure which exploits this solution by assembling
concentrically a number of such topological defects can establish a flat stellar or galactic rotation curve, and can also deflect
light in the same manner as an equipotential (isothermal) sphere. Thus, the need for dark matter or modified gravity theory is
mitigated, at least in part.
Or: Beyond linear.
Abstract: Equivariant neural networks are neural networks that incorporate symmetries. The nonlinear activation functions in these networks result in interesting nonlinear equivariant maps between simple representations, and motivate the key player of this talk: piecewise linear representation theory.
Disclaimer: No one is perfect, so please mind that there might be mistakes and typos.
dtubbenhauer@gmail.com
Corrected slides: dtubbenhauer.com/talks.html
Describing and Interpreting an Immersive Learning Case with the Immersion Cub...Leonel Morgado
Current descriptions of immersive learning cases are often difficult or impossible to compare. This is due to a myriad of different options on what details to include, which aspects are relevant, and on the descriptive approaches employed. Also, these aspects often combine very specific details with more general guidelines or indicate intents and rationales without clarifying their implementation. In this paper we provide a method to describe immersive learning cases that is structured to enable comparisons, yet flexible enough to allow researchers and practitioners to decide which aspects to include. This method leverages a taxonomy that classifies educational aspects at three levels (uses, practices, and strategies) and then utilizes two frameworks, the Immersive Learning Brain and the Immersion Cube, to enable a structured description and interpretation of immersive learning cases. The method is then demonstrated on a published immersive learning case on training for wind turbine maintenance using virtual reality. Applying the method results in a structured artifact, the Immersive Learning Case Sheet, that tags the case with its proximal uses, practices, and strategies, and refines the free text case description to ensure that matching details are included. This contribution is thus a case description method in support of future comparative research of immersive learning cases. We then discuss how the resulting description and interpretation can be leveraged to change immersion learning cases, by enriching them (considering low-effort changes or additions) or innovating (exploring more challenging avenues of transformation). The method holds significant promise to support better-grounded research in immersive learning.
When I was asked to give a companion lecture in support of ‘The Philosophy of Science’ (https://shorturl.at/4pUXz) I decided not to walk through the detail of the many methodologies in order of use. Instead, I chose to employ a long standing, and ongoing, scientific development as an exemplar. And so, I chose the ever evolving story of Thermodynamics as a scientific investigation at its best.
Conducted over a period of >200 years, Thermodynamics R&D, and application, benefitted from the highest levels of professionalism, collaboration, and technical thoroughness. New layers of application, methodology, and practice were made possible by the progressive advance of technology. In turn, this has seen measurement and modelling accuracy continually improved at a micro and macro level.
Perhaps most importantly, Thermodynamics rapidly became a primary tool in the advance of applied science/engineering/technology, spanning micro-tech, to aerospace and cosmology. I can think of no better a story to illustrate the breadth of scientific methodologies and applications at their best.
The cost of acquiring information by natural selectionCarl Bergstrom
This is a short talk that I gave at the Banff International Research Station workshop on Modeling and Theory in Population Biology. The idea is to try to understand how the burden of natural selection relates to the amount of information that selection puts into the genome.
It's based on the first part of this research paper:
The cost of information acquisition by natural selection
Ryan Seamus McGee, Olivia Kosterlitz, Artem Kaznatcheev, Benjamin Kerr, Carl T. Bergstrom
bioRxiv 2022.07.02.498577; doi: https://doi.org/10.1101/2022.07.02.498577
3. History of Chloroform
Chloroform was first prepared in 1831 by an
American chemist Dr. Samuel Guthrie, who
combined whisky with chlorinated lime in an
attempt to produce a cheap pesticide.
4. Preparation of Chloroform
Chloroform is prepared in the laboratory by heating ethanol with bleaching
powder. The reaction is called haloform reaction.
When a paste of bleaching powder is heated with ethanol, chloroform is
obtained. The reaction takes place in the following steps :
• Step 1 : CaOCl2 + H2O Cl2 + Ca(OH)2
(Bleaching Powder)
• Step 2 : Chlorine thus obtained acts as both oxidising and chlorinating
agent. It first oxidises ethanal into acetaldehyde and then chlorinates
acetaldehyde to give trichloroacetaldehyde (chloral).
5. Step 3 : Trichloroacetaldehyde thus formed is
hydrolysed by calcium hydroxide to give chloroform.
6. Properties of Chloroform
• It is a colourless and heavy liquid with a peculiar sickly
smell and sweetish burning taste.
• It is heavier than water
• It is generally insoluble in water, but soluble in most
organic solvents.
• Boiling Point : 334 K & Freezing Point : 210 K
• It’s vapours burns with a green edged flame.
• It’s vapours when inhaled, causes temporary
unconsciousness. Therefore, formerly, it is used as an
anaesthetic.
• It is toxic in nature. It is no longer in use.
7. Uses of Chloroform
• It is used as an anaesthetic. As it’s slightly overdoses
are dangerously toxic, its use as an anaesthetic is not
much preferred. Now-a-days, it has been replaced by
other more safe anaesthetics.
• It is used as a solvent for dyes and pesticides.
• It is used for the preservation of dead bodies and
anatomical specimens.
• It is used in medicines.
• It is used as a laboratory reagent.
8. Facts Related to Chloroform
When Chloroform comes in contact with
direct sunlight, it converts into
Phosgene, which is highly poisonous.
Phosgene is used in World War I (WW1)
as a chemical weapon.