Question

Which one of the following reactions will not result in the formation of a carbon-carbon bond?
(A) Reimer- Tiemann reaction
(B) Friedel Crafts acylation
(C) Wurtz reaction
(D) Cannizzaro reaction

Answer 1

The formation of the new C-C bond in the product, such that a new carbon atom or group is added to the reactant carbon. Thus, generating new bonds during the reaction. So, it can only be seen through the reaction mechanism of the given reactions.

Complete step by step solution:
The given reactions take place as follows:
- In Reimer- Tiemann reaction, the phenol reacts with the chloroform in the presence of a strong base like sodium hydroxide to give salicylaldehyde. That is, the addition of $-CHO$ group on the benzene ring of phenol and thus, the formation of a new C-C bond.

- In Friedel Crafts acylation reaction, the arene reacts with the acyl chloride or the anhydride in the presence of aluminium chloride as the catalyst, leading to the formation of aryl ketone. That is, addition of the $-COR$ group on the benzene ring and thus, formation of a new C-C bond.

- In Wurtz reaction, the alkyl halide is treated with sodium metal in the presence of dry ether to form higher alkanes. Thus, addition of two alkyl groups, forming a new C-C bond.
$R-X\xrightarrow[dry\,\,ether]{Na}R-R+2NaX$
- In Cannizzaro reaction, the non-$\alpha -H$ aldehydes undergo a self- redox reaction in the presence of a strong base like NaOH, to form an alcohol and carboxylic acid through disproportionation, thus no new C-C bond is formed. 2RCHO\xrightarrow[{{H}_{3}}{{O}^{+}}]{NaOH}RC{{H}_{2}}OH+RCOOH

Therefore, in the given reactions, the option (D)- Cannizzaro reaction will not result in the formation of carbon-carbon bonds.

Note: In reaction (A) and (B), it is seen that the new C-C bond is formed by the addition of the carbonyl group to the aromatic benzene ring. Whereas, in reaction (C) it simply involves the addition of the alkyl group of the alkyl halide reactant species to another.