Stereochemistry and aromaticity UE Past Papers Questions.


View All Courses

(3689) Question Category: Multiple choices

In chair conformers of substituted eyelohexane large substituent groups prefer

  1. The axial position to avoid 1,3 diaxial interactions
  2. The equatorial position to avoid 1,2 diaxial interactions
  3. The axial position to avoid 1.3 diaxial interactions
  4. The equatorial position to avoid 1,3 diaxial interaction

Answer / Solution

UNSOLVED

(3690) Question Category: Multiple choices

How many chiral centers are in the molecule with the formula CH_{3}CHFCHFCH(CH_{3})_{2}

  1. 2
  2. 3
  3. 4
  4. 8

Answer / Solution

UNSOLVED

(3691) Question Category: Multiple choices

Cis and trans isomers of 1,2-dichloroethane have;

  1. The same boiling point
  2. Different melting point
  3. The same level of polarity
  4. Different density

Answer / Solution

UNSOLVED

(3692) Question Category: Multiple choices

Suppose you are provided with R-thalidomine and S-thalidomine, what is streochemical relationship of the two compounds.

  1. Diastereomers
  2. Optical isomers
  3. Enantiomers
  4. Enatiomeric pure drug

Answer / Solution

UNSOLVED

(3693) Question Category: Multiple choices

Cyclopropane when burnt in air produces more energy than propane due to;

  1. Higher molecular weight of cyclopropane
  2. Angle strain
  3. Higher intermolecular forces in cyclopropane
  4. Unreactive state of cyclopropane.

Answer / Solution

UNSOLVED


View All Courses
News & Updates | Recently
Recent Updates
questions

2024-05-02: questions

Questions Uploaded on 2024-05-02


questions

2024-03-29: questions

Questions Uploaded on 2024-03-29


questions

2024-03-19: questions

Questions Uploaded on 2024-03-19

Dismissible in 10 seconds