CameraIcon

SearchIcon

MyQuestionIcon

1

You visited us 1 times! Enjoying our articles? Unlock Full Access!

Other Reductions

An organic ac...

Question

An organic acid P $C_{11} H_{12} O_{2}$ can easily be oxidized to a dibasic acid which reacts with ethylene glycol to produce a polymer dacron. Upon ozonolysis, P gives an aliphatic ketone as one of the products. P undergoes the following reaction sequences to furnish R via Q. The compound P also undergoes another set of reactions to produce S.

The compound R is :

A

Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses

B

No worries! We‘ve got your back. Try BYJU‘S free classes today!

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 A

Suggest Corrections

thumbs-up

0

Similar questions

Q. A carbonyl compound P, which gives positive iodoform test, undergoes reaction with MeMgBr followed by dehydration to give an olefin Q. Ozonolysis of Q leads to a dicarbonyl compound R, which undergoes intra-molecular aldol reaction to give predominantly S.

The structures of the products S, is

The structure of the carbonyl compound P, which gives positive iodoform test undergoes reaction with MeMgBr followed by dehydration to give an olefin Q. Ozonolysis of Q leads to a dicarbonyl compound R, which undergoes intramolecular aldol reaction to give predominantly S.

The structure of the carbonyl compound P is:

Q. A carbonyl compound P (from i-iii), which gives positive iodoform test, undergoes with MeMgBr followed by dehydration to give an olefin Q. Ozonolysis of Q leads to a dicarbonyl compound R, which undergoes intramolecular aldol reaction to give predominantly S.

2. Product S is :

Q. A carbonyl compound P, which gives positive iodoform test, undergoes reaction with MeMgBr followed by dehydration to given an olefin Q. Ozonolysis of Q leads to a dicarbonyl compound R, which undergoes intramolecular-aldol reaction to give predominantly S.

P = 1. M e M g B r - --------------- \to 2. H^{+}, H_{2} O 3. H_{2} S O_{4} / h e a t Q 2. O_{3} / Z n - H_{2} O - -------- \to R O H^{-} - -- \to h e a t S

The structure of the carbonyl compound P, is

Q. A carbonyl compound P, which gives positive iodoform test, undergoes reaction with MeMgBr followed by dehydration to given an olefin Q. Ozonolysis of Q leads to a dicarbonyl compound R, which undergoes intramolecular-aldol reaction to give predominantly S.

P = 1. M e M g B r - --------------- \to 2. H^{+}, H_{2} O 3. H_{2} S O_{4} / h e a t Q 2. O_{3} / Z n - H_{2} O - -------- \to R O H^{-} - -- \to h e a t S

The structure of the product S, is

View More

Join BYJU'S Learning Program

similar_icon

Related Videos

lock

Reduction of Carboxylic Acids and its Derivatives

CHEMISTRY

Watch in App

explore_more_icon

Explore more

Other Reductions

Standard XII Chemistry

Join BYJU'S Learning Program

CrossIcon