/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q45P How could you convert butanenitr... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

How could you convert butanenitrile into the following compounds?

Write each step showing the reagents needed.

(a) 1-Butanol

(b) Butylamine

(c) 2-Methyl-3-hexanone

Short Answer

Expert verified

The conversion of the butanenitrile into following compounds can be explained.

Step by step solution

01

Conversion of Butanenitrile into 1-Butanol

The conversion of butanenitrile into butanoic acid when base can hydrolyse. The treatment of butanoic acid with LiAlH4 follows the acidification and reduced into 1-butanol. The steps involved are,

CH3CH2CH2CN→H2ONaOHCH3CH2CH2CO2H→2.H3O+1.LiAlH4CH3CH2CH2CH2OH

02

Conversion of Butanenitrile into Butylamine

The treatment of butanenitrile with LiAlH4 follows the acidification and reduced into butylamine. The steps involved are,

CH3CH2CH2CN→2.H3O+1.LiAlH4CH3CH2CH2CH2NH2

03

Conversion of Butanenitrile into 2-Methyl-3-hexanone

The treatment of butanenitrile with isopropylmagnesium in addition to Grignard reagent to triple bond. There is a formation of intermediate in hydrolysis using 2-methyl-3-hexanone. The steps involved are,

CH3CH2CH2CN→2.H3O+1.(CH3)2CHMgBrCH3CH2CH2C∥OC|CH3HCH3

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Study anywhere. Anytime. Across all devices.