Geometrical isomerism is caused by-
1. Restricted rotation around C=C bond.
2. The presence of one asymmetric carbon atom.
3. The different groups attached to the same functional group.
4. None of the above.
The compounds that show geometrical isomerism among the following are:
a. 2-Butene
b. Propene
c. 1-Phenylpropene
d. 2-Methylbut-2-ene
1. a, b
2. c, d
3. a, b, c
4. a, c
The chiral compound among the following is:
1. | 2-Methylpentanoic acid | 2. | Pentanoic acid |
3. | 4-Methyl pentanoic acid | 4. | None of the above |
But-2-ene exhibits cis-trans isomerism due to-
1. Rotation around sigma bond
2. Rotation around bond
3. Restricted rotation around C=C bond
4. Rotation around double bond
The structure of diphenylmethane is given below:
The number of structural isomers possible when one of the hydrogen atom is replaced by a chlorine atom are :
1. | 6 | 2. | 4 |
3. | 8 | 4. | 7 |
The optically active compound among the following is-
1. Butane
2. 2-Methyl pentane
3. 4-Methyl pentane
4. 3-Methyl hexane
The maximum number of stereoisomers possible for 3-hydroxy-2-methyl butanoic acid is/are :
1. 1
2. 2
3. 3
4. 4
Glucose and fructose are-
1. | Chain isomers | 2. | Position isomers |
3. | Functional isomers | 4. | Optical isomers |
The optically active compound among the following is-
1. | Glycerine | 2. | Acetaldehyde |
3. | Glyceraldehyde | 4. | Acetone |