answersLogoWhite

0


Best Answer

in basic medium m-nitrobenzoic acid reacts with methanol to form methyl m-nitrobenzoate

User Avatar

Wiki User

14y ago
This answer is:
User Avatar
More answers
User Avatar

AnswerBot

5mo ago

m-Nitrobenzoic acid can be converted into methyl m-nitrobenzoate by reacting it with methanol and an acid catalyst such as sulfuric acid. The reaction is an esterification process that involves combining the m-nitrobenzoic acid with methanol to form the corresponding ester, methyl m-nitrobenzoate, and water as a by-product. This reaction is commonly carried out under reflux conditions to drive the reaction to completion.

This answer is:
User Avatar

User Avatar

Wiki User

13y ago

methyl m-nitrobenzoate. TLC analysis shows it moves more slowly up the plate.

This answer is:
User Avatar

User Avatar

Wiki User

14y ago

nitrobenzene isn't water soluble

This answer is:
User Avatar

Add your answer:

Earn +20 pts
Q: How do you convert m-nitrobenzoic acid into methyl m-nitrobenzoate?
Write your answer...
Submit
Still have questions?
magnify glass
imp
Related questions

How do you convert methyl chloride to ethyl chloride?

Methyl chloride can be converted to ethyl chloride by reacting it with ethyl alcohol (ethanol) in the presence of an acid catalyst, such as sulfuric acid. The reaction is an SN1 substitution reaction where the methyl group on methyl chloride is replaced by an ethyl group from ethanol, forming ethyl chloride. The reaction proceeds via the formation of a carbocation intermediate.


Which is more acidic butanoic acid or 3 methyl butanoic acid?

3-methyl butanoic acid is more acidic than butanoic acid because the presence of the methyl group in 3-methyl butanoic acid increases the electron-withdrawing effect, making the molecule more acidic by stabilizing the conjugate base.


What is more polar methyl salicylate or salicylic acid?

salicylic acid (an acid) is more polar than methyl salicylate (an ester)


How do you prepare methyl 2 methyl butyrate?

Methyl 2-methylbutyrate can be prepared by the esterification of 2-methylbutyric acid with methanol in the presence of a strong acid catalyst, such as sulfuric acid. The reaction is usually carried out under reflux conditions and the ester is then isolated by extraction and distillation.


Is methyl isocyanate MIC an acid or an alkali?

Acid. i think.


How do you distinguish 2-methyl-3-nitrobenzoic acid from3-methyl-2-nitrobenzoic acid?

You can distinguish between the two compounds by using spectroscopic techniques, such as NMR or IR spectroscopy, which can help identify the positions of the substituents on the benzene ring. Additionally, you can use chemical reactions specific to each compound, like derivatization reactions or selective reduction reactions, to differentiate between 2-methyl-3-nitrobenzoic acid and 3-methyl-2-nitrobenzoic acid.


What is the reactions of hydrochloric acid to methyl orange?

Hydrochloric acid is an acid, so it reacts with methyl orange, which is a pH indicator. When added to hydrochloric acid, methyl orange turns red due to the low pH of the acid. This color change indicates the presence of an acidic solution.


What amino acid has a methyl group as its R group?

Alanine is the amino acid with a methyl group as its R group.


Is Butyl Alcohol a reactants used to make methyl butyrate?

Yes, butyl alcohol can be used as a reactant to make methyl butyrate through esterification. Butyl alcohol reacts with butyric acid to form methyl butyrate and water.


What is the common name for methyl propionate?

The common name for methyl propionate is propionic acid methyl ester.


What is pH methyl orange in acid?

3.1 to 4.4 depending on the concentration of the acid.


What acid is present in beef and mutton?

Methyl heptadecanoic acid is present in mutton.