CameraIcon
CameraIcon
SearchIcon
MyQuestionIcon
MyQuestionIcon
1
You visited us 1 times! Enjoying our articles? Unlock Full Access!
Question

Given below are two statements:

Statement I: The nucleophilic addition of sodium hydrogen sulphite to an aldehyde or a ketone involves proton transfer to form a stable ion.

Statement II: The nuceophilic addition of hydrogen cyanide to an aldehyde or a ketone yields amine as final product.

In the light of the above statements, choose the most appropriate answer from the options given below:

A
Statement I is false but statement II is true
No worries! We‘ve got your back. Try BYJU‘S free classes today!
B
Statement I is true but statement II is false
Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses
C
Both Statement I and Statement II are true
No worries! We‘ve got your back. Try BYJU‘S free classes today!
D
Both Statement I and Statement II are false
No worries! We‘ve got your back. Try BYJU‘S free classes today!
Open in App
Solution

The correct option is B Statement I is true but statement II is false
Sodium hydrogensulphite (NaHSO3)adds to aldehydes and ketones to form the addition products. The hydrogensulphite addition compound is water soluble and can be converted back to the original carbonyl compound by treating it with dilute mineral acid or alkali.

Hence, option (a) is correct.

Mechanism of addition of NaHSO3 involves 2 steps.
Step-1: Nucleophilic attack on ​carbonyl carbon:
Step-2: Formation of an adduct

flag
Suggest Corrections
thumbs-up
7
Join BYJU'S Learning Program
similar_icon
Related Videos
thumbnail
lock
Synthesis of Ethers
CHEMISTRY
Watch in App
Join BYJU'S Learning Program
CrossIcon