The product in the above reaction is:

1.
2.
3.
4.	This reaction cannot take place

Organic compounds sometimes adjust their electronic as well as steric structures to attain stability. Among the following, the compounds having the highest dipole moments is

1.  

2.  

3.  

4.  

Terpinene-4-ol, an active ingredient in tea tree oil, has the following structure:

The correct observations for terpinene-4-ol are:

1. I, II, III, and IV

2. I, III, and IV

3. II and III

4. III and IV

Addition of bromine to cis-3-hexene gives

1.  Racemic dibromide

2.  A mixture of diastereomeric dibromides

3.  Optically active dibromide

4.  Meso dibromide

Among the following compounds the one that is most reactive towards electrophilic nitration is

1. Benzoic acid

2. Nitrobenzene

3. Toluene

4. Benzene

Some meta-directing substituents in aromatic substitution are given. Which one is the most deactivating?

Consider the following reaction:
  
What is the major product A?

1.		2.
3.		4.

1. Phenol

2. Aniline

3. Methoxy benzene

4. Toluene

Which of the following would exhibit cis-trans isomerism?

1. ${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{CH}={\mathrm{CH}}_2$

2. $\mathrm{ClCH}=\mathrm{CHCl}$

3. $\mathrm{ClCH}={\mathrm{CCl}}_2$

4. ${\mathrm{CH}}_2=\mathrm{CH}-\mathrm{COOH}$

The non-aromatic compound among the following is-

1.            

2.

3.         

 4.