When O chlorotoluene is treated with sodium amide The product is?

Question: When m-chlorotoluene is treated with sodium amide in liquid ammonia, the products of the reaction are o-, m-, and p-toluidine (i.e. o-CH3C6H4NH2, m-CH3C6H4NH2 and p-CH3C6H4NH2).

Which of the following compounds is the major product when o chlorotoluene reacts with sodamide in presence of ammonia?

o-Chlorotoluene reacts with sodamide in liquid NH_(3) to give o-toluidine and m-toluidine.

What is the reaction product between Bromotoluene and sodium amide?

Reaction of ortho-bromotoluene with sodium amide in liquid ammonia produces two major products, ortho-toluidine (i.e., 2-methylaniline) and meta-toluidine (i.e., 3-methylaniline).

What happen when chlorobenzene is treated with Sodamide in liquid ammonia?

When chlorobenzene is treated with NaNH2in liquid ammonia at 196K, aniline is formed.

When toluene is subjected to Etard reaction the product formed is?

Limitations. The Étard reaction is most commonly used as a relatively easy method of converting toluene into benzaldehyde.

What happens when toluene reacts with cl2?

Complete step by step answer: Toluene is basically methyl substituted benzene. When the reaction takes place in light the substitution occurs on the methyl group instead of benzene ring, hence 3 hydrogen of alkyl group het substituted by 3 hydrogen and trichloromethyl benzene forms.

What is the formula of Sodamide?

NaNH2
Sodium amide/Formula

What type of reaction is Etard reaction?

The Étard reaction is a chemical reaction that involves the direct oxidation of an aromatic or heterocyclic bound methyl group to an aldehyde using chromyl chloride.

When toluene is treated with chromyl chloride in CS2 it forms benzaldehyde the reaction is called?

The oxidation of toluene (C6​H5​CH3​ with chromyl chloride (CRO2​Cl2​) in CCl4​ or CS2​ to give benzaldehyde is called Etard reaction. In this reaction, the chromyl chloride first forms a brown complex, which is seperated and then decomposed with H2​O to give benzaldehyde (C6​H5​CHO).

What happens when methylbenzene is treated with chlorine in the presence of light?

If chlorine or bromine react with boiling methylbenzene in the absence of a catalyst but in the presence of UV light, substitution happens in the methyl group rather than the ring. However, the reaction doesn’t stop there, and all three hydrogens in the methyl group can in turn be replaced by chlorine atoms.

What happens when toluene react with cl2 in the presence of fecl3 catalyst?

When toluene reacts with chlorine in the presence of ferric chloride it gives o-chlorotoluene and para-toluene and hydrochloride as the products. The major products formed in this reaction are o-chlorotoluene and p-chlorotoluene.

What happens when sodium is added to liquid ammonia?

Liquid ammonia can serve a variety of purposes depending from reaction to reaction. Add sodium to it, the solution will turn blue. Add sodium to a larger excess of liquid ammonia, it’ll turn brown.

What happens when an alkane reacts with chlorine gas?

Except chlorine radicals in a well-known reaction. Chlorine radicals, which are essentially chlorine atoms formed as a product when chlorine gas undergoes homolytic fission in UV, attacks the alkane as an electrophile and strips away a H along with an electron.

Are C-H bonds in alkanes electrophilic?

C-H bonds in alkanes are not polarized and therefore generally unable to attract any electrophiles or nuclophiles. Except chlorine radicals in a well-known reaction.

What is the chemical reaction between alkane and iodine?

Chlorine radicals, which are essentially chlorine atoms formed as a product when chlorine gas undergoes homolytic fission in UV, attacks the alkane as an electrophile and strips away a H along with an electron. Iodine most probably undergo the same fission under UV since I-I bonds are weaker than Cl-Cl bonds.