Which of the following sequence will convert 3-phenylbutanenitrile to 3-phenylbutan-1-ol?

1 – workup

2 – $H_{2} O, H^{+}, Δ$

3 – reduction with $L i A l H_{4}$

3; 2; 1

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

2; 3; 1

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

3; 1; 2

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

1; 2; 3

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

Open in App

Solution

The correct option is B
2; 3; 1

Acid hydrolysis converts the nitrile into a carboxylic acid, which on reduction with $L i A l H_{4}$ followed by a workup gives 3-phenylbutan-1-ol:

Suggest Corrections

Similar questions

Which of the following sequence will convert 3-phenylbutanenitrile to 3-phenylbutan-1-ol?

1 – workup

2 – $H_{2} O, H^{+}, Δ$

3 – reduction with $L i A l H_{4}$

Which of the following sequence converts benzaldehyde into phenylacetaldehyde?

1: $P B r_{3}$
2: Mg in THF
3: $N a B H_{4} f o l l o w e d b y H_{3} O^{+}$
4: $H C H O f o l l o w e d b y H_{3} O^{+}$
5: PCC

Q. Find the correct option(s) considering the following reactions sequence:

Given: Vapor density of C is 29 and E is anesthetic in nature.

Look at this enamine:

Which of the following sequence converts benzaldehyde into the given enamine?

1: Oxidation with Cr(VI) compound
2: reaction with pyrrolidine with pH control; acid catalyst
3: $M e M g B r f o l l o w e d b y H_{3} O^{+}$

Q. Which of the esters shown, after reduction with

{L i A l H}_{4}

and aqueous workup, will yield two molecules of only a single alcohol ?

Join BYJU'S Learning Program

Which of the following sequence will convert 3-phenylbutanenitrile to 3-phenylbutan-1-ol? 1 – workup 2 – H2O,H+,Δ 3 – reduction with LiAlH4

The correct option is B 2; 3; 1 Acid hydrolysis converts the nitrile into a carboxylic acid, which on reduction with LiAlH4 followed by a workup gives 3-phenylbutan-1-ol:

Which of the following sequence will convert 3-phenylbutanenitrile to 3-phenylbutan-1-ol?

1 – workup

2 – $H_{2} O, H^{+}, Δ$

3 – reduction with $L i A l H_{4}$

The correct option is B
2; 3; 1

Acid hydrolysis converts the nitrile into a carboxylic acid, which on reduction with $L i A l H_{4}$ followed by a workup gives 3-phenylbutan-1-ol: