Chemistry Chapter 15 Entry Test MCQs

(A) CH3CH2CH2CH2Br (B) CH3CH2CHBrCH3 (C) (CH3)3CBr with alcoholic KOH is

a.
b.
c.
d.

a. CH3CH = CHCH3
b. CH3CH = CHCH3
c. (CH3)2CHCH2OCH2CH3
d. CH3CH2CH(OCH2CH3)CH3

b. CH3CH = CHCH3

a.
b.
c.
d.

a. RCl < RBr < RI
b. RI < RBr < RCl
c. RCl < RI < RBr
d. RI < RCl < RBr

a. RCl < RBr < RI

a. 1-butene
b. 2-hydroxybutane
c. 2-butene
d. butanol

c. 2-butene

a. one molecule of alkyl halide and one molecule of aldehyde
b. two molecules of alkyl halides
c. two molecules of aryl halides
d. one molecule of each of alkyl and aryl halide

d. one molecule of each of alkyl and aryl halide

a. Predominantly 1–butane
b. Equimolar mixture of 1 and 2–butene
c. 2–butyne
d. Predominantly 2–butene

d. Predominantly 2–butene

a. Protic solvent
b. Stability of R+
c. Aprotic solvent
d. Steric hindrance

d. Steric hindrance

a. CH3Cl
b. CH3F
c. CH3I
d. CH3Br

b. CH3F

a.
b.
c.
d.

a. Reaction with PCl3
b. Reaction with HX in the presence ZnCl2
c. Reaction with PCl5
d. Reaction with SOCl2 in the presence of pyridine solvent

d. Reaction with SOCl2 in the presence of pyridine solvent

a. 2-butene
b. 1-butanol
c. 1-butyne
d. 1-butene

d. 1-butene

a. Stability of the carbonium ion
b. Nucleophilicity of the attacking nucleophile
c. The nature of leaving group
d. Solvent system

b. Nucleophilicity of the attacking nucleophile

a. Propyne
b. 1,2-dibromopropane
c. Propene
d. Propane

a. Propyne

a. SN1 reaction
b. SN2 reaction
c. E1 reaction
d. E2 reaction

c. E1 reaction

a. Hybridization of C in transition state
b. Nature of alkyl group
c. Kinetics of the reaction
d. Nature of solvent

a. Hybridization of C in transition state

a. Reaction is single step due to least stearic hindrance
b. It is unimolecular reaction
c. It is a bimolecular reaction because it occurs in two steps
d. Rate depends upon the formation of carbonium ion

a. Reaction is single step due to least stearic hindrance

a.
b.
c.
d.

a. Secondary butyl iodide
b. neopentyl chloride
c. t-butyl chloride
d. Isobutyl bromide

c. t-butyl chloride

a. methanol
b. Methyl chloride
c. ethanol
d. Ethyl chloride

d. Ethyl chloride

a. Rate or reaction
b. Order of reaction
c. Extent of a reaction
d. Molecularity of a reaction

d. Molecularity of a reaction

a. Neutral
b. Positive
c. Negative
d. Both b and c

b. Positive

Grignard`s Reagent

a. A carbon chain attached to a metal
b. A carbon chain attached to magnesium
c. A carbon chain with an alcohol on the end
d. A carbon double bonded to an oxygen

b. A carbon chain attached to magnesium

a. Ethyl iodide
b. Methyl amine
c. Ethyl alcohol
d. Diethyl ether

a. Ethyl iodide

a. Halogen
b. Methyl group
c. -COOH group
d. Magnesium

c. -COOH group

a. Propanal
b. Propane
c. Propanol
d. Propanoic acid

d. Propanoic acid

a. Warming them with Mg powder in dry ether
b. Boiling them with Mg ribbon in alcoholic solution
c. Warming them with MgCl2
d. Refluxing them with MgCl2 solution

a. Warming them with Mg powder in dry ether

a. Carbon free radical
b. Carbocation
c. Carbene
d. Carbanion

d. Carbanion

a. Tertiary alcohol
b. Primary alcohol
c. and aldehyde
d. Secondary alcohol

a. Tertiary alcohol

a. Pentanal
b. Butyl formate
c. Methyl butanoate
d. 3- pentanone

a. Pentanal

a. 4-heptanone
b. 3-methylpentanal
c. Acetone
d. Cyclohexanone

b. 3-methylpentanal

a. Propanone
b. Formaldehyde
c. Carbon dioxide
d. Acetaldehyde

c. Carbon dioxide

a. Acetone
b. 2-Butanone
c. 2-Pentanone
d. 3-Pentanone

a. Acetone

a. a mixture of benzene and Mg(OMe)Br
b. a mixture of anisole and Mg(OH)Br
c. a mixture of phenol and Mg(Me)Br
d. a mixture of toluene and Mg(OH)Br

a. a mixture of benzene and Mg(OMe)Br

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