Chemistry - Organic Chemistry MCQS

A. Hydroxyl (-OH)
B. Carbonyl (C=O)
C. Amino (-NH₂)
D. Ester (-COO-)
A. Acetic acid
B. Propionic acid
C. Butanoic acid
D. Ethanoic acid
A. Reduction
B. Oxidation
C. Hydrolysis
D. Esterification
A. Stereoisomerism
B. Structural isomerism
C. Geometric isomerism
D. Optical isomerism
A. Carbonyl (C=O)
B. Hydroxyl (-OH)
C. Carboxyl (-COOH)
D. Amino (-NH₂)
A. CnH₂n
B. CnH2n+2
C. CnH2n-2
D. CnHn
A. CH₃OH
B. CH₃CH₂OH
C. (CH₃)₂CHOH
D. CH₃COOH
A. Pentane
B. Butane
C. Hexane
D. Propane
A. Ether (-O-)
B. Aldehyde (C=O)
C. Carboxylic acid (-COOH)
D. Amine (-NH₂)
A. sp²
B. sp³
C. sp
D. sp⁴
A. Aldehyde
B. Ketone
C. Carboxylic acid
D. Ester
A. Esterification
B. Hydrolysis
C. Saponification
D. Dehydration
A. Propanal
B. Butanal
C. Pentanal
D. Ethanal
A. CnH₂n+2
B. CnH2n
C. CnH2n-2
D. CnHn
A. Halogenation
B. Hydrogenation
C. Dehydration
D. Oxidation
A. Ethene
B. Propane
C. Benzene
D. Butyne
A. Butanol
B. Ethanol
C. Propanol
D. Pentanol
A. CH₃NH₂
B. (CH₃)₂NH
C. NH₃
D. C₆H₅NH₂
A. Alkene
B. Aldehyde
C. Ketone
D. Ether
A. Carboxyl (-COOH)
B. Carbonyl (C=O)
C. Hydroxyl (-OH)
D. Ester (-COO-)
A. Combustion
B. Halogenation
C. Hydrolysis
D. Oxidation
A. Acetone
B. Propanone
C. Butanone
D. Ethanal
A. Ethylamine
B. Propylamine
C. Butylamine
D. Ethylmethanamine
A. Structural isomerism
B. Stereoisomerism
C. Geometric isomerism
D. Optical isomerism
A. sp
B. sp²
C. sp³
D. sp⁴
A. Esterification
B. Transesterification
C. Saponification
D. Hydrolysis
A. Hexane
B. Butane
C. Pentane
D. Octane
A. CH₃OH
B. CH₃CH₂OH
C. (CH₃)₃COH
D. CH₃COOH
A. Halogenation
B. Hydrogenation
C. Dehydration
D. Oxidation
A. Butanone
B. Pentanone
C. Hexanone
D. Propanone
A. Ethene
B. Propene
C. Butene
D. Butadiene
A. Ethylamine
B. Propylamine
C. Butylamine
D. Ethylmethanamine
A. Carbonyl (C=O)
B. Hydroxyl (-OH)
C. Carboxyl (-COOH)
D. Amino (-NH₂)
A. Alkane
B. Alkene
C. Alkyne
D. Dihalide
A. Geometric isomerism
B. Structural isomerism
C. Stereoisomerism
D. Optical isomerism
A. Ethyl acetate
B. Methyl acetate
C. Butyl acetate
D. Propyl acetate
A. Hydrogenation
B. Hydration
C. Halogenation
D. Dehydration
A. CH₃NH₂
B. (CH₃)₂NH
C. NH₃
D. C₆H₅NH₂
A. Halogenation
B. Hydrogenation
C. Dehydration
D. Oxidation
A. Methyl ethylamine
B. Ethyl methylamine
C. Dimethylamine
D. Diethylamine
A. Amide (-CONH₂)
B. Carbonyl (C=O)
C. Hydroxyl (-OH)
D. Ester (-COO-)
A. Methyl propanoate
B. Ethyl methanoate
C. Propyl ethanoate
D. Ethyl propanoate
A. Reduction
B. Oxidation
C. Hydrolysis
D. Esterification
A. Epoxidation
B. Hydrogenation
C. Hydration
D. Halogenation
A. Propylamide
B. Butanamide
C. Pentanamide
D. Ethylamide
A. Esterification
B. Transesterification
C. Saponification
D. Hydrolysis
A. Ethene
B. Propene
C. Butene
D. Ethyne
A. Butanone
B. Pentanone
C. Hexanone
D. Propanone
A. Halogenation
B. Hydration
C. Dehydration
D. Halide substitution
A. Ethylamine
B. Propylamine
C. Butylamine
D. Ethylmethanamine
A. Ethylene glycol
B. Propylene glycol
C. Glycerol
D. Butane-1,3-diol
A. Hydrogenation
B. Halogenation
C. Hydration
D. Markovnikov addition
A. Methyl propanoate
B. Ethyl methanoate
C. Propyl ethanoate
D. Ethyl propanoate
A. Ozonolysis
B. Hydrogenation
C. Hydration
D. Halogenation
A. Butanoic acid
B. Ethanoic acid
C. Propanoic acid
D. Pentanoic acid
A. HCl
B. H₂O
C. BF₃
D. NH₃
A. Acetone
B. Propanone
C. Butanone
D. Ethanal
A. Hydrogenation
B. Halogenation
C. Hydration
D. Dehydration
A. Ethylamine
B. Propylamine
C. Butylamine
D. Methanamine
A. Halogenation
B. Hydrogenation
C. Hydration
D. Dehydration
A. Ethanol
B. Propanol
C. Butanol
D. Isopropanol
A. Hydrogenation
B. Halogenation
C. Hydration
D. Dehydration
A. Butanone
B. Pentanone
C. Hexanone
D. Propanone
A. Halogenation
B. Hydrogenation
C. Hydration
D. Anti-Markovnikov addition
A. Butanoic acid
B. Ethanoic acid
C. Propanoic acid
D. Pentanoic acid