1
MCQ (Single Correct Answer)

JEE Main 2018 (Online) 15th April Evening Slot

Two compounds I and II are eluted by column chromatography (adsorption of I > II). Which one of following is a correct statement ?
A
I moves faster and has higher Rf value than II
B
II movesfaster and has higher  Rf  value than I
C
I moves slower and has higher  Rf  value than II
D
II moves slower and has higher  Rf  value than I

Explanation

According to question,

Absorption of I > II, it means I is firmly attached to column. Hence it will move slowly and move little distance. As II is loosely attached to column.

So, it will move faster and will move larger distance.
2
MCQ (Single Correct Answer)

JEE Main 2018 (Online) 15th April Evening Slot

On treatment of the following compound with a strong acid, the most susceptible site for bond cleavage is :

A
Cl $$-$$ O2
B
O2 $$-$$ C3
C
C4 $$-$$ O5
D
O5 $$-$$ C6

Explanation

Here the lone pair of electrons on O2 is involved in resonace with C = C.
So,   O2 will not be protonated.

The lone pair electrons of O5 is not involved in resonance with any C = C. So, O5 can be protonated.

When we use strong acid like HCl then chloride ion will attack least substituted C atom (C6).

3
MCQ (Single Correct Answer)

JEE Main 2018 (Online) 16th April Morning Slot

The most polar compound among the following is :
A
B
C
D
4
MCQ (Single Correct Answer)

JEE Main 2019 (Online) 9th January Morning Slot

Arrange the following amines in the decreasing order of basicity :

A
I > II > III
B
III > I > II
C
III > II > I
D
I > III > II

Explanation



Baric nature depends on the tendency of donating the lone pair.

In (I) st amine lone pair of N atom is not in resonance. So it can easily donate the lone pair.

In (II) amine lone pair of N atom is in resonance. So, lone pair is not available.

In (III) amine lone pair of N atom is not in resonance so lone pair can be easily donated.

So, (I) and (III) are more baric compare to (II).

In (I) amine N atom is connected to sp2 hybridised carbon atom and in (III) amine N atom is connected to sp3 hybridised carbon atom.

We know sp2 carbon atom has more $$-$$ I effect than sp3 carbon atom.

So, in (I) amine density of electrons around N atom will decrease due to $$-$$ I effect and basic nature also decrease.

So, correct order of basic nature : III > I > II

Questions Asked from Basics of Organic Chemistry

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