ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES AND TECHNIQUES|, Exams of Organic Chemistry

Hybridisation of an atom-H = No. of σ bonds + No. of lone pairs Selection of Principle Carbon Chain-1. Principal functional group 2. Maximum number of multiple bonds 3. Maximum number of Carbon atoms 4. Maximum number of substituents Carboxylic acids--COOH -oic acid Sulphonic acids--SO3H -sulphonic acid Acid anhydride-R-C(=O)-O-C(=O)-R -oic anhydride Esters-RCOOR -oate Acid halides-RCOX oyl halide

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2025/2026

Available from 04/13/2026

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ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES AND
TECHNIQUES|VERIFIED ANSWERS100%|2025
Hybridisation of an atom-✓✓H = No. of σ bonds + No. of lone pairs
Selection of Principle Carbon Chain-✓✓1. Principal functional group
2. Maximum number of multiple bonds
3. Maximum number of Carbon atoms
4. Maximum number of substituents
Carboxylic acids-✓✓-COOH
-oic acid
Sulphonic acids-✓✓-SO3H
-sulphonic acid
Acid anhydride-✓✓R-C(=O)-O-C(=O)-R
-oic anhydride
Esters-✓✓RCOOR
-oate
Acid halides-✓✓RCOX
oyl halide
Amides-✓✓RCONH2
-amide
Nitriles-✓✓R-CN
-nitrile
Aldehydes-✓✓-CHO
-al
Ketones-✓✓C=O
-one
Alcohols-✓✓R-OH
-ol
Thiols-✓✓R-SH
-thiol
Amines-✓✓-NH2
-Amine
Alkyl-✓✓-R
pf2

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ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES AND

TECHNIQUES|VERIFIED ANSWERS100%|

Hybridisation of an atom-✓✓H = No. of σ bonds + No. of lone pairs Selection of Principle Carbon Chain-✓✓1. Principal functional group

  1. Maximum number of multiple bonds
  2. Maximum number of Carbon atoms
  3. Maximum number of substituents Carboxylic acids-✓✓-COOH -oic acid Sulphonic acids-✓✓-SO3H -sulphonic acid Acid anhydride-✓✓R-C(=O)-O-C(=O)-R -oic anhydride Esters-✓✓RCOOR -oate Acid halides-✓✓RCOX oyl halide Amides-✓✓RCONH -amide Nitriles-✓✓R-CN -nitrile Aldehydes-✓✓-CHO -al Ketones-✓✓C=O -one Alcohols-✓✓R-OH -ol Thiols-✓✓R-SH -thiol Amines-✓✓-NH -Amine Alkyl-✓✓-R

Halo-✓✓-X Hydroxy-✓✓-OH Alkoxy (Ether)-✓✓-OR Amino-✓✓-NH Cyano-✓✓-CN Formyl or oxo-✓✓-CHO Oxo-✓✓>C=O Carboxy-✓✓-COOH Nitro-✓✓-NO As Electronegativity increases-✓✓Stability of carbanion increases, stability of carbocation decreases Stability of Carbocation α-✓✓+I/-I Stability of Carbanion α-✓✓-I/+I