Home
Class 12
CHEMISTRY
Controlled oxidation of primary alcohols...

Controlled oxidation of primary alcohols give

A

aldehydes

B

ketones

C

carboxylic acids

D

ethers

Text Solution

Verified by Experts

The correct Answer is:
A
Doubtnut Promotions Banner Mobile Dark
|

Topper's Solved these Questions

  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -5|1 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -6|1 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -3|1 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH SERIES|Exercise ETHERS (OBJECTIVE EXERCISE-4)|50 Videos
  • ALKYL AND ARYL HALIDES

    AAKASH SERIES|Exercise OBJECTIVE EXERCISE - 4 (ASSERTION (A) & REASON (R) TYPE QUESTIONS)|19 Videos

Similar Questions

Explore conceptually related problems

Under what circumstances may an aldehyde be prepared by oxidation of primary , alcohol, with acid dichromate ?

Name the reagents used in the Oxidation of primary alcohol to carboxylic acid reaction.

Knowledge Check

  • Controller oxidation of primary alcobols gives

    A
    aldehydes
    B
    ketones
    C
    carboxylic acids
    D
    ethers
  • Oxidation of primary alcohols finally gives

    A
    Aldehydes
    B
    Ketones
    C
    Carboxylic acids
    D
    Esters
  • Oxidation of primary Alcohols finally gives

    A
    Aldehydes
    B
    Ketones
    C
    Carboxylic acids
    D
    Esters
  • Similar Questions

    Explore conceptually related problems

    Name the reagents used in the Oxidation of primary alcohol to aldehyde reaction.

    1 Name the reagents used in the following reactions: (i) Oxidation of a primary alcohol to carboxylic acid. (ii) Oxidation of a primary alcohol to aldehyde. (iii) Bromination of phenol to 2,4,6-tribromophenol. (iv) Benzyl alcohol to benzoic acid. (v) Dehydration of propan-2-ol to propene. (vi) Butan-2-one to butan-2-ol.

    A better reagent for oxidation of primary alcohols to aldehydes in good yield is

    (A): Oxidation of tertiary alcohols requires strong oxidising agent and elevated temperature. (R): Oxidation of tertiary alcohols involves cleavage of C - C bond.

    Dehydrogenation of isopropyl alcohol gives