$CH_3CH(I)_2$ $\xrightarrow{KCN}$ $\xrightarrow[\Delta]{H_3O^{+}} ?$ Here the end product would be

  • A
    $2-$Cyano propionic acid
  • B
    Ethane$-1,1-$dicarboxylic acid
  • C
    $2-$Methyl ethanoic acid
  • D
    Propionic acid

Explore More

Similar Questions

All of the following compounds react with ethylmagnesium bromide $(CH_3CH_2MgBr)$. Alcohols are formed from three of the compounds. Which one does not give an alcohol?

Lower members of aliphatic carboxylic acids are soluble in water. This is due to

Which of the following is most reactive towards nucleophilic attack at the carbonyl group?

Which of the following esters,after reduction with $LiAlH_4$ followed by aqueous workup,will yield two molecules of only a single alcohol?

When carboxylic acid reacts with organolithium reagents to give ketones,side reactions sometimes occur. For example,
$HOCH_2CH_2CH(CH_3)CH_2CH_2COOH$ $\xrightarrow[(x) \, CH_3Li]{tetrahydro\,furan}$ $\xrightarrow[NH_4Cl]{H_2O}$ $\underset{63\%}{\text{Compound } A: HOCH_2CH_2CH(CH_3)CH_2CH_2COCH_3}$ + $\underset{37\%}{\text{Compound } (B)}$
The value of $(x)$ in the above reaction is:

Difficult
View Solution

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo