Embibe Experts Solutions for Chapter: Aldehydes, Ketones and Carboxylic Acids, Exercise 1: AMU-AT (B.Tech.) 2018

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Embibe Experts Chemistry Solutions for Exercise - Embibe Experts Solutions for Chapter: Aldehydes, Ketones and Carboxylic Acids, Exercise 1: AMU-AT (B.Tech.) 2018

Attempt the free practice questions on Chapter 25: Aldehydes, Ketones and Carboxylic Acids, Exercise 1: AMU-AT (B.Tech.) 2018 with hints and solutions to strengthen your understanding. EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY solutions are prepared by Experienced Embibe Experts.

Questions from Embibe Experts Solutions for Chapter: Aldehydes, Ketones and Carboxylic Acids, Exercise 1: AMU-AT (B.Tech.) 2018 with Hints & Solutions

EASY
AMU-AT (B.Tech.)
IMPORTANT

Cinnamic acid is formed when C6H5-CHO condenses with CH3CO2O in presence of

EASY
AMU-AT (B.Tech.)
IMPORTANT

Aldehydes and ketones can be reduced to hydrocarbon by using

EASY
AMU-AT (B.Tech.)
IMPORTANT

On heating an aldehyde with Fehling's reagent, a reddish brown precipitate is obtained due to the formation of

MEDIUM
AMU-AT (B.Tech.)
IMPORTANT

A compound C5H10O(A) forms a phenylhydrazone and gives negative Tollen's test and a positive Iodoform reaction. It also gives n-pentane on reduction. The compound (A) is

MEDIUM
AMU-AT (B.Tech.)
IMPORTANT

A β -hydroxy carbonyl compound is obtained by the action of NaOH on

EASY
AMU-AT (B.Tech.)
IMPORTANT

Name the end product in the following series of reactions S ections

Question Image

EASY
AMU-AT (B.Tech.)
IMPORTANT

The most reactive to nucleophilic attack at the carbonyl group is