• NEET
      • Class 11th
      • Class 12th
      • Class 12th Plus
    • JEE
      • Class 11th
      • Class 12th
      • Class 12th Plus
    • Class 6-10
      • Class 6th
      • Class 7th
      • Class 8th
      • Class 9th
      • Class 10th
    • View All Options
      • Online Courses
      • Distance Learning
      • Hindi Medium Courses
      • International Olympiad
    • NEET
      • Class 11th
      • Class 12th
      • Class 12th Plus
    • JEE (Main+Advanced)
      • Class 11th
      • Class 12th
      • Class 12th Plus
    • JEE Main
      • Class 11th
      • Class 12th
      • Class 12th Plus
  • Classroom
  • NEW
    • NEET
      • 2025
      • 2024
      • 2023
      • 2022
    • JEE
      • 2025
      • 2024
      • 2023
      • 2022
    • Class 6-10
    • JEE Main
      • Previous Year Papers
      • Sample Papers
      • Result
      • Analysis
      • Syllabus
      • Exam Date
    • JEE Advanced
      • Previous Year Papers
      • Sample Papers
      • Mock Test
      • Result
      • Analysis
      • Syllabus
      • Exam Date
    • NEET
      • Previous Year Papers
      • Sample Papers
      • Mock Test
      • Result
      • Analysis
      • Syllabus
      • Exam Date
      • College Predictor
      • Counselling
    • NCERT Solutions
      • Class 6
      • Class 7
      • Class 8
      • Class 9
      • Class 10
      • Class 11
      • Class 12
    • CBSE
      • Notes
      • Sample Papers
      • Question Papers
    • Olympiad
      • NSO
      • IMO
      • NMTC
    • TALLENTEX
    • AOSAT
  • ALLEN E-Store
    • ALLEN for Schools
    • About ALLEN
    • Blogs
    • News
    • Careers
    • Request a call back
    • Book home demo
Home
Class 12
CHEMISTRY
Reimer-Tiemann reaction introduces an al...

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below:

Which one of the following reagents is used in the above reaction ?

To view this video, please enable JavaScript and consider upgrading to a web browser thatsupports HTML5 video

Doubtnut Promotions Banner Desktop LightDoubtnut Promotions Banner Desktop DarkDoubtnut Promotions Banner Mobile LightDoubtnut Promotions Banner Mobile Dark

Text Solution

Verified by Experts

The correct Answer is:
C
NA

Topper's Solved these Questions

  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Archives Multiple Correct|4 Videos

  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Archives Fill In The Blanks|6 Videos

  • ALCOHOL,PHENOL AND ETHERS

    CENGAGE CHEMISTRY|Exercise Archives Assertion-Reasoning|2 Videos

  • ALIPHATIC AND AROMATIC ALDEHYDES AND KETONES

    CENGAGE CHEMISTRY|Exercise Archives Subjective|29 Videos

Similar Questions

Explore conceptually related problems

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below:

The electrophile in this reaction is:

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below:

The structure of the intremediate (I) is:

Reimer Tiemann reaction introduces an aldehyde group, on to the ring of phenol, ortho to hydroxyl group. The reaction involves electro-philic aromatic substitution. This is a general method for synthesis of substituted salicyladehyde as depicted below

Which one of the following reagents is used in the above reactions

Reimer Tiemann reaction introduces an aldehyde group, on to the ring of phenol, ortho to hydroxyl group. The reaction involves electro-philic aromatic substitution. This is a general method for synthesis of substituted salicyladehyde as depicted below The electrophile in this reaction is

Reimer Tiemann reaction introduces an aldehyde group, on to the ring of phenol, ortho to hydroxyl group. The reaction involves electro-philic aromatic substitution. This is a general method for synthesis of substituted salicyladehyde as depicted below

The structure of the intermediate is

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. Thi reaction involves electrophilic aromatic substitution. It is a general method for the synthesis of substituted salicylaldehydes as depicted below: Q. Which one of the following reagents is used ini the above reaction?


Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. Thi reaction involves electrophilic aromatic substitution. It is a general method for the synthesis of substituted salicylaldehydes as depicted below:
Q. The electrophilic in this reaction is-

Riemer-Tiemann reaction intorduces an aldehyde group, on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substitued salicyladehydes as depicted below. The structure of the intermediate I is:

Reimer -Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substituted salicyladehydes as depicted below.

The electrophile in this reaction is

Reimer -Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substituted salicyladehydes as depicted below. The structure of the intermediate I is

Reimer-Tiemann reaction introduces an aldehyde group, on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substituted salicyladehydes as depicted below. Which one of the following reagents is used in the above reaction ?

Reimer-Tiemann reaction introduces an aldehyde group, on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substituted salicyladehydes as depicted below. The electrophile in this reaction is

Reimer-Tiemann reaction introduces an aldehyde group, on to the aromatic ring of phenol, ortho to the hydroxyl group. This reaction involves electrophilic aromatic substitution. This is a general method for the synthesis of substituted salicyladehydes as depicted below.

The structure of the intermediate I is

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below:

Which one of the following reagents is used in the above reaction ?

Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below: The electrophile in this reaction is:

CENGAGE CHEMISTRY-ALCOHOL,PHENOL AND ETHERS-Archives Linked Comprehension
  1. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

    03:14

    |

  2. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

    03:29

    |

  3. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

    04:37

    |

Home
Profile
|