(a) How do you convert the following:
(i) Phenol to anisole

(ii) Ethanol to propan-2-ol

(b) write the mechanism of the following reaction:

(c) Why phenol undergoes electrophilic substitution more easily than benzene?

OR

(a) Account for the following:

(i) O-nitrophenol is more steam volatile than p-nitrophenol

(ii) T-butyl chloride on heating with sodium methoxide gives 2-methylpropene instead of t-butylmethylether.

(b) Write the reaction involved in the following:

(i) Reamer-Tiemann reaction

(ii) Friedel-Crafts alkylation of phenol

(c) Give simple chemical test to distinguish between ethanol and phenol.

Question

(a) How do you convert the following:
(i) Phenol to anisole

(ii) Ethanol to propan-2-ol

(b) write the mechanism of the following reaction:

(c) Why phenol undergoes electrophilic substitution more easily than benzene?

OR

(a) Account for the following:

(i) O-nitrophenol is more steam volatile than p-nitrophenol

(ii) T-butyl chloride on heating with sodium methoxide gives 2-methylpropene instead of t-butylmethylether.

(b) Write the reaction involved in the following:

(i) Reamer-Tiemann reaction

(ii) Friedel-Crafts alkylation of phenol

(c) Give simple chemical test to distinguish between ethanol and phenol.

Philoid · Accepted Answer

(a) (i)

Phenol when treated with aqueous NaOH gives soidmum phenoxide ion which when treatment with methyl bromide or methyl iodide to give anisole as the product.

Rxn:

(a) (ii)

The primary and most efficient way to create a 2° alcohol is by using Grignard’s reagent. For that we need to convert ethanol into an aldehyde which can be done by partial oxidation of alcohols. This is done with the help of pyridinium chlorochromate (PCC) or by using chromic acid CrO₃.

Rxn:

Acetaldehyde on treatment with Grignard’s reagent and then hydrolysis will give a secondary alcohol.

(b) Mechanism of elimination reaction from alcohols.

Step 1: Protonation of alcohols

Step 2: Removal of water molecule/ generation of carbocation

Step 3: De-protonation of ethylium ion

(c) –OH group is o-p directing and oxygen atom has two lone pairs that show positive resonance which increases the electron density over benzene. The C ─ O gains partial double bond character during the resonance that increases the strength of the bond and thus is difficult to break under normal conditions. This decreases its tendency to accept any more electrons and favours electrophilic substitution of Hydrogen atoms instead of nucleophilic substitution

OR

(a) (i)

In case of o-nitrophenol, it undergoes hydrogen bonding that involve six atom geometry (most stable form of hydrogen bonding) as shown in the figure given below.

The hydrogen bonding increases the intramolecular attraction and in turn decreases the boiling point of o-nitrophenol.

In case of p-nitrophenol it undergoes intermolecular hydrogen bonding which increases the boiling point. Thus o-nitrophenol is more steam volatile than p-nitrophenol.

(a) (ii)

Formation of ether proceeds with attack of alkaoxide ion. This ion is large and the alkyl substituents on the tert-butyl alcohol create stearic hindrance in order to reach the oxygen atom. Also sodium methoxide is a strong base and hence a S_N¹ mechanism is preferred over breaking of O─H bond, and elimination predominates over substitution reaction.

(b) (i) Reimer-Tiemann reaction

Phenol when treated with chloroform in aq. NaOH gives a dichlorocarbene electrophile that attacks the phenol ring at ortho-position. When this intermediate treated with NaOH forms a sodium salt of salicylaldehyde which on hydrolysis will give salicylaldehyde as the main product.

(b) (ii) Friedel Crafts reaction of phenol

When phenol is treated with a lewis acid and alkyl halide it undergoes electrophilic substitution reaction to give o-cresol and p-cresol as the major product.