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

Phenol reacts with methyl chloroformate in the presence of NaOH to form product A. A reacts with Br2 to form product B. A and B are respectively


A
No worries! We‘ve got your back. Try BYJU‘S free classes today!
B
Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses
C
No worries! We‘ve got your back. Try BYJU‘S free classes today!
D
No worries! We‘ve got your back. Try BYJU‘S free classes today!
Open in App
Solution

The correct option is B

The explanation for the correct option:

Option (B):

  1. Sodium hydroxide, a strong base, removes the proton from phenol to create the phenoxide ion. The carbonyl carbon of methyl chloroformate, which is an electron-deficient carbon, is attacked by phenoxide ion, an electron-rich species.
  2. As a result, methyl chloroformate's chlorine ion was removed. Compound A is produced as a result of this.
  3. After compound A is created, it interacts with Br2 to create compound B. The electron density is pushed into the para position by compound A's functional group, a para-directing group. As a result, the combination forms compound B, which attacks Br2 via its para location.
  4. Hence, it is the correct option.

Therefore, A and B are


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