HARD
Earn 100

Find out number of reactions those proceed with retention of the configuration.

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Important Questions on Organic Compounds Containing Halogens

EASY
Consider the reaction
CH3CH2CH2Br+NaCNCH3CH2CH2CN+NaBr
This reaction will be the fastest in
MEDIUM
Compound (A), C8H9Cl, gives a white precipitate when warmed with alcoholic AgNO3. Oxidation of (A) gives an acid (B), C8H6O4. (B) easily forms anhydride on heating. Identify the compound (A).
MEDIUM
How do you distinguish chlorobenzene from benzyl chloride?
MEDIUM
The major product obtained in the following reaction is,

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EASY

The reagent required for the following two step transformation are

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MEDIUM
In SN2 reactions, the correct order of reactivity for the following compounds :
CH3Cl, CH3CH2Cl, (CH3)2CHCl and (CH3)3CCl is :
MEDIUM

The increasing order of reactivity of the following compounds towards reaction with alkyl halides directly is:

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(ii)  Question Image

(iii) Question Image

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EASY
The increasing order of the reactivity of the following halides for the SN1 reaction is

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MEDIUM

In the reaction given below what will be the major product at the end :

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EASY
Which of the following, upon treatment with tert-BuONa  followed by addition of bromine water, fails to decolourize the colour of bromine?
EASY
Which of the following compounds shall not produce propene by reaction with HBr followed by elimination or direct only elimination reaction?
MEDIUM
Neopentyl bromide, undergoes dehydrohalogenation to give alkenes even though it has no βH . This is due to
MEDIUM
The order of SN1 reactivity in aqueous acetic acid solution for the compounds
(1) H 3 C - C || O - C H 2 - C l

(2) H3C-CH2-CH2-Cl

(3) H3C3C-Cl

is
EASY
For the following reactions:
a. CH3CH2CH2Br + KOH CH3CH=CH2+ KBr+ H2O 
b.
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c.
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Which of the following statements is correct?
MEDIUM
Which of the following will most readily give the dehydrohalogenation product?