Predict the products of the following reactions:
$(i)$ Cyclopentanone + $NH_2OH \xrightarrow{H^+} ?$
(ii) Cyclohexanone + $2,4-DNP \xrightarrow{H^+} ?$
(iii) $R-CH=CH-CHO + NH_2CONHNH_2 \xrightarrow{H^+} ?$
(iv) Acetophenone + $CH_3CH_2NH_2 \xrightarrow{H^+} ?$

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) The reactions involve the nucleophilic addition of ammonia derivatives to carbonyl compounds followed by the elimination of a water molecule to form imine derivatives.
$(i)$ Cyclopentanone + $NH_2OH \xrightarrow{H^+} \text{Cyclopentanone oxime} + H_2O$
(ii) Cyclohexanone + $2,4-DNP \xrightarrow{H^+} \text{Cyclohexanone-2,4-dinitrophenylhydrazone} + H_2O$
(iii) $R-CH=CH-CHO + NH_2CONHNH_2 \xrightarrow{H^+} R-CH=CH-CH=NNHCONH_2 + H_2O$
(iv) Acetophenone + $CH_3CH_2NH_2 \xrightarrow{H^+} \text{N-ethylacetophenone imine} + H_2O$

Explore More

Similar Questions

What products are formed on the reaction of $Propanal$ with $2-Methylpropanal$ in the presence of $NaOH$? Write the name of the reaction.

Nucleophilic addition reaction will be most favoured in

Given below are two statements:
Statement $I$: Cross aldol condensation between two different aldehydes will always produce four different products.
Statement $II$: When semicarbazide reacts with a mixture of benzaldehyde and acetophenone under optimum pH, it forms a condensation product with acetophenone only.
In the light of the above statements, choose the correct answer from the options given below:

Write a note on the preparation of secondary alcohols from ketones by reduction reaction.

Identify the compounds $A$ and $B$ involved in the formation of the given aldol product: $A + B \xrightarrow{OH^-} CH_3-CH_2-CH(OH)-CH(CH_3)-CHO$

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