The IUPAC name of the following compound is
1. 4-hydrazonocyclohexane-1-carboxylic acid
2. 4-hydrazonobenzoic acid
3. 4-hydrazonocyclohexanoic acid
4. 4-(n-amino) benzene carboxylic acid
Consider the following organic compound,
To make it a chiral compound, the attack should be on carbon.
1. 1
2. 4
3. 3
4. 7
Assign the IUPAC name for the following compound.
1. 3, 4-Dichlorobenzene
2. (4-chlorophenyl)(3-chlorophenyl) diazene
3. 3,4-Bis (chlorophenyl) diazene
4. (3-Chlorophenyl)(4-chlorophenyl)diazene
Assign the IUPAC name for the following compound.
1. 3-methyl hexane -1, 2, 3-tricarbonitrile
2. hexane-1, 2, 3-tricarbonitrile
3. 1, 2-bis(cyanomethyl) butanenitrile
4. 3-(cyanomethyl)hexane-1,6-dinitrile
The number of chiral carbon atoms in the given compound is are
1. 2
2. 3
3. 4
4. 1
In the following reaction,
an asymmetric center is generated. The acid obtained would be
1. L-isomer
2. D-isomer
3. 20% D+ 80% L-isomer
4. 50% D+ 50 % L-isomer
Hybridization is applicable on a set among the following from left to right is -
1.
2.
3.
4.
The hydrocarbons having the lowest dipole moment among the following is:
1.
2. CH3 - C ≡ C - CH3
3. CH3 CH2 CH = CH2
4. CH2 = CH - C ≡ CH
In the compound, the bond is of the type
1.
2.
3.
4.
An organic compound is found to be optically active. Which of the following is the correct structure of the given compound?
1.
2.
3.
4.