Organic chemistry involves the study of the structure, properties, composition, reactions, and preparation of carbon-containing compounds, which include not only hydrocarbons but also compounds with any number of other elements, including hydrogen (most compounds contain at least one carbon–hydrogen bond), nitrogen, oxygen, halogens, phosphorus, silicon, and sulfur.
This branch of chemistry was originally limited to compounds produced by living organisms but has been broadened to include human-made substances such as plastics. The range of application of organic compounds is enormous and also includes, but is not limited to, pharmaceuticals, petrochemicals, food, explosives, paints, and cosmetics.
This is a report about Aldehydes. The content of this slideshow are as follows: What is an aldehyde, How to name aldehydes with IUPAC Nomenclature and Common Names, The Physical Properties of Aldehydes, and the examples of aldehyde and its uses. The main objective of this report is to widen the knowledge of the readers/learners concerning of the stated topic so that they can further understand the concept of aldehydes.
Report made by: Students of Sogod National High School STEM 9-Newton
Kyla Krystelle Salva
Krishia Belle Cambalon
Marycris Felicilda
HSSC Second year Chemistry course slides for Federal Board Pakistan, lectures by Dr. Raja Hashim Ali (also available on Youtube as lecture videos).
https://www.youtube.com/playlist?list=PLCfCZszhGHBeEx8MuI5EkN1QHmpanhZra
Alcohol, phenol, and ether are organic compounds that play significant roles in both natural processes and synthetic chemistry. In the NCERT Class 12 Chemistry curriculum, the study of these compounds forms a crucial part of the organic chemistry syllabus. This essay aims to provide a comprehensive analysis of alcohol, phenol, and ether, as outlined in the NCERT textbooks. Beginning with fundamental concepts such as nomenclature and classification, we will delve into the structural properties, chemical reactivity, synthesis methods, and practical applications of these compounds. Additionally, we will explore advanced topics such as reactions mechanisms, stereochemistry, and spectroscopic analysis, thereby offering a holistic understanding of alcohol, phenol, and ether chemistry.
Introduction:
Alcohol, phenol, and ether represent a diverse group of organic compounds characterized by the presence of hydroxyl (–OH) and/or ether (–O–) functional groups. These compounds exhibit unique chemical properties and find wide-ranging applications in industry, medicine, and everyday life. The NCERT Class 12 Chemistry curriculum provides students with a systematic framework for understanding the structure, properties, and reactions of alcohols, phenols, and ethers. This essay aims to elucidate the key concepts covered in this curriculum, thereby fostering a deeper appreciation for the chemistry of these important functional groups.
I. Basic Concepts and Nomenclature:
A. Definition and Classification of Alcohols, Phenols, and Ethers
B. IUPAC Nomenclature Rules and Examples
C. Structural Isomerism and Functional Group Isomerism
II. Structure and Bonding:
A. Molecular Structure of Alcohols, Phenols, and Ethers
B. Intermolecular Forces: Hydrogen Bonding in Alcohols and Phenols
C. Dipole-Dipole Interactions in Ethers
III. Chemical Properties and Reactivity:
A. Acid-Base Behavior: Alcohols and Phenols as Weak Acids
B. Nucleophilic Substitution Reactions: SN1 and SN2 Mechanisms
C. Esterification and Ether Cleavage Reactions
D. Oxidation and Reduction Reactions: Preparation of Aldehydes, Ketones, and Carboxylic Acids
IV. Synthetic Methods:
A. Laboratory Preparation of Alcohols: Hydration of Alkenes, Reduction of Aldehydes and Ketones
B. Industrial Synthesis of Phenol: Cumene Process
C. Williamson Ether Synthesis and Other Methods for Ether Preparation
V. Stereochemistry of Alcohols and Ethers:
A. Chirality and Enantiomerism
B. Optical Activity and Chiral Centers in Alcohols
C. Conformational Isomerism in Ethers
VI. Spectroscopic Analysis:
A. IR Spectroscopy: Characteristic Peaks for Alcohols, Phenols, and Ethers
B. NMR Spectroscopy: Chemical Shifts and Signal Splitting Patterns
C. Mass Spectrometry: Fragmentation Patterns and Molecular Weight Determination
VII. Applications and Industrial Importance:
A. Alcohol as Solvents and Antiseptics
B. Phenol in the Production of Polymers and Pharmaceuticals
C. Ethers as Solvents and Anesthetic Agents
Organic chemistry involves the study of the structure, properties, composition, reactions, and preparation of carbon-containing compounds, which include not only hydrocarbons but also compounds with any number of other elements, including hydrogen (most compounds contain at least one carbon–hydrogen bond), nitrogen, oxygen, halogens, phosphorus, silicon, and sulfur.
This branch of chemistry was originally limited to compounds produced by living organisms but has been broadened to include human-made substances such as plastics. The range of application of organic compounds is enormous and also includes, but is not limited to, pharmaceuticals, petrochemicals, food, explosives, paints, and cosmetics.
This is a report about Aldehydes. The content of this slideshow are as follows: What is an aldehyde, How to name aldehydes with IUPAC Nomenclature and Common Names, The Physical Properties of Aldehydes, and the examples of aldehyde and its uses. The main objective of this report is to widen the knowledge of the readers/learners concerning of the stated topic so that they can further understand the concept of aldehydes.
Report made by: Students of Sogod National High School STEM 9-Newton
Kyla Krystelle Salva
Krishia Belle Cambalon
Marycris Felicilda
HSSC Second year Chemistry course slides for Federal Board Pakistan, lectures by Dr. Raja Hashim Ali (also available on Youtube as lecture videos).
https://www.youtube.com/playlist?list=PLCfCZszhGHBeEx8MuI5EkN1QHmpanhZra
Alcohol, phenol, and ether are organic compounds that play significant roles in both natural processes and synthetic chemistry. In the NCERT Class 12 Chemistry curriculum, the study of these compounds forms a crucial part of the organic chemistry syllabus. This essay aims to provide a comprehensive analysis of alcohol, phenol, and ether, as outlined in the NCERT textbooks. Beginning with fundamental concepts such as nomenclature and classification, we will delve into the structural properties, chemical reactivity, synthesis methods, and practical applications of these compounds. Additionally, we will explore advanced topics such as reactions mechanisms, stereochemistry, and spectroscopic analysis, thereby offering a holistic understanding of alcohol, phenol, and ether chemistry.
Introduction:
Alcohol, phenol, and ether represent a diverse group of organic compounds characterized by the presence of hydroxyl (–OH) and/or ether (–O–) functional groups. These compounds exhibit unique chemical properties and find wide-ranging applications in industry, medicine, and everyday life. The NCERT Class 12 Chemistry curriculum provides students with a systematic framework for understanding the structure, properties, and reactions of alcohols, phenols, and ethers. This essay aims to elucidate the key concepts covered in this curriculum, thereby fostering a deeper appreciation for the chemistry of these important functional groups.
I. Basic Concepts and Nomenclature:
A. Definition and Classification of Alcohols, Phenols, and Ethers
B. IUPAC Nomenclature Rules and Examples
C. Structural Isomerism and Functional Group Isomerism
II. Structure and Bonding:
A. Molecular Structure of Alcohols, Phenols, and Ethers
B. Intermolecular Forces: Hydrogen Bonding in Alcohols and Phenols
C. Dipole-Dipole Interactions in Ethers
III. Chemical Properties and Reactivity:
A. Acid-Base Behavior: Alcohols and Phenols as Weak Acids
B. Nucleophilic Substitution Reactions: SN1 and SN2 Mechanisms
C. Esterification and Ether Cleavage Reactions
D. Oxidation and Reduction Reactions: Preparation of Aldehydes, Ketones, and Carboxylic Acids
IV. Synthetic Methods:
A. Laboratory Preparation of Alcohols: Hydration of Alkenes, Reduction of Aldehydes and Ketones
B. Industrial Synthesis of Phenol: Cumene Process
C. Williamson Ether Synthesis and Other Methods for Ether Preparation
V. Stereochemistry of Alcohols and Ethers:
A. Chirality and Enantiomerism
B. Optical Activity and Chiral Centers in Alcohols
C. Conformational Isomerism in Ethers
VI. Spectroscopic Analysis:
A. IR Spectroscopy: Characteristic Peaks for Alcohols, Phenols, and Ethers
B. NMR Spectroscopy: Chemical Shifts and Signal Splitting Patterns
C. Mass Spectrometry: Fragmentation Patterns and Molecular Weight Determination
VII. Applications and Industrial Importance:
A. Alcohol as Solvents and Antiseptics
B. Phenol in the Production of Polymers and Pharmaceuticals
C. Ethers as Solvents and Anesthetic Agents
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
In this webinar you will learn how your organization can access TechSoup's wide variety of product discount and donation programs. From hardware to software, we'll give you a tour of the tools available to help your nonprofit with productivity, collaboration, financial management, donor tracking, security, and more.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Introduction to AI for Nonprofits with Tapp NetworkTechSoup
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Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
2. IUPAC nomenclature system
International Union for Pure and Applied Chemistry
(IUPAC)
• An IUPAC name is given to a compound based on the
name of its parent alkane.
prefix - parent - suffix
• Step 1:
• Draw the structural formula of the straight chain compound
and count the number of carbon atoms in it.
• Write the name of this alkane.
• If the compound contains a double bond OR a triple bond
change the ending of the parent's name from ‘ane’ to ‘ene’ OR
from ‘ane’ to ‘yne’.
3. IUPAC nomenclature system
International Union for Pure and Applied Chemistry
(IUPAC)
• Step 2: If the structural formula contains a functional group
replaces the last letter ‘e’ from the parent's name with the
condensed name of the functional group as the suffix.
(Exception: The condensed name of the functional group
‘halogen’ is always attached as the prefix.)
• Step 3: Number the carbon atoms in the carbon chain from
one end to the other. Assign the number ‘1’ to carbon in the
functional group -CHO or -COOH, if present, Otherwise, the
chain can be numbered in two directions. Accept that
numbering which gives a smaller number to the carbon
carrying the functional group. In the final name, a digit
(number) and a character (letter) should be separated by a
small horizontal line
6. Important carbon compounds
• Ethanol:
• At room temperature colourless ethanol is a liquid
• its boiling points is 78 0C.
• Generally ethanol is called alcohol or spirit.
• Ethanol is soluble in water in all proportions.
• When aqueous solution of ethanol is tested with litmus paper it is found to be
neutral.
• Consumption of small quantities of dilute ethanol shows its effect, even though is
condemned still it has remained a socially widespread practice. Consumption of
alcohol harms health in a number of ways.
• It adversely affects the physiological processes and the central nervous system.
Consumption of even a small quantity of pure ethanol (called absolute alcohol) can
be lethal. Ethanol being a good solvent, it is used in medicines such as tincture iodine
(solution of iodine and ethanol), cough mixture, and also in many tonics.
7. Chemical properties of ethanol
• Reaction with sodium
2Na + 2CH3-CH2- OH 2 CH3-CH2-ONa+ H2
All the alcohols react with sodium metal to liberate hydrogen gas and form
sodium alkoxide salts. In the reaction of ethanol with sodium metal, hydrogen
gas and sodium ethaoxide are formed as products.
8. Chemical properties of ethanol
• Dehydration reaction: When ethanol is heated at the temperature
170 0C with an excess amount of concentrated sulphuric acid, one
molecule of water is removed from its molecule to form ethene, an
unsaturated compound.
CH3-CH2-OH CH2=CH2 + H2O
• Here, concentrated sulphuric acid acts as a dehydrating agent.
9. Important carbon compounds
• Ethanoic acid:
• Ethanoic acid is a colourless liquid with boiling point1180C.
• Ethanoic acid is commonly known as acetic acid.
• Its aqueous solution is acidic and turns blue litmus red.
• Vineger, which is used as preservative in pickles, is a 5-8 % aqueous solution
of acetic acid.
• The melting point of pure ethanoic acid is 170 0C . Therefore, during winter in
cold countries ethanoic acid freezes at room temperature itself and looks like
ice. Therefore it is named ‘glacial acetic acid’.
10. Chemical properties of ethanoic acid
• Reaction with base
• A reaction with strong base
• Ethanoic acid gives neutralization reaction with a strong base sodium
hydroxide to form a salt and water.
CH3-COOH + NaOH CH3-COO Na + H2O
• The IUPAC name of the salt formed here is sodium ethanoate while
it’s common name is sodium acetate.
11. Chemical properties of ethanoic acid
• Reaction with carbonate and bicarbonate
• Ethanoic acid reacts with the basic salt, namely, sodium carbonate, to form a
salt , named sodium ethanoate, water and carbon dioxide gas.
• The CO2 gas of the effervescence passes through the gas delivery tube and
reacts with the lime water in the small test tube. ‘Lime water turning milky’ is
the test of carbon dioxide gas. If sodium bicarbonate is used instead of
sodium carboanate in the above activity, similar observation are obtained.
CH3COOH + NaHCO3 CH3COONa+ H2O + CO2