Is nitroaniline an acid?

Is nitroaniline an acid?

3-Nitroaniline is an aniline carrying a nitro functional group in position 3. It is stable in neutral, acidic or alkaline solutions and is classified as “not readily biodegradable” with “low bioaccumulation potential”.

Is nitroaniline an amine?

Nitroaniline is an organic chemical compound consisting of a phenyl group and an amino group. Nitroaniline occurs as a stable, water-soluble powder that ranges from yellow to brown in color and gives off a slightly amine aroma.

What is the structure of m-nitroaniline?

C6H6N2O23-Nitroaniline / Formula

What is the use of acetanilide?

acetanilide, synthetic organic compound introduced in therapy in 1886 as a fever-reducing drug. Its effectiveness in relieving pain was discovered soon thereafter, and it was used as an alternative to aspirin for many years in treating such common complaints as headache, menstrual cramps, and rheumatism.

What is the functional group of 4 nitroaniline?

A nitroaniline carrying a nitro group at position 4. 4-Nitroaniline, p-nitroaniline or 1-amino-4-nitrobenzene is an organic compound with the formula C6H6N2O2. A yellow solid, it is one of three isomers of nitroaniline.

What is Odour of M nitro aniline?

2-Nitroaniline

PubChem CID 6946
Synonyms 2-NITROANILINE o-Nitroaniline 88-74-4 Benzenamine, 2-nitro- 2-Nitrobenzenamine More…
Molecular Weight 138.12
Dates Modify 2022-03-04 Create 2005-03-26
Description O-nitroaniline is an orange solid with a musty odor. Sinks and mixes slowly with water. (USCG, 1999) CAMEO Chemicals

Is 4 nitroaniline water soluble?

4-Nitroaniline

Names
Melting point 146 to 149 °C (295 to 300 °F; 419 to 422 K) (lit.)
Boiling point 332 °C (630 °F; 605 K)
Solubility in water 0.8 mg/ml at 18.5 °C (IPCS)
Vapor pressure 0.00002 mmHg (20°C)

Does M-nitroaniline dissolve in water?

When the aqueous layer has 6 M NaOH added to you, the m-nitroaniline is regenerated, and since it is now insoluble in water, you can collect it as a solid.

Why was acetanilide discontinued?

Acetanilide was used in the 19th century to treat fever and headaches but was discontinued because of toxic side effects.

Is acetanilide electron withdrawing or donating?

1 Answer. linu f. Amide group in acetanilide is donating group to benzene, and the amide group in N-methylbenzamide is electron withdrawing group.