You nitrate the benzene with nitric and sulfuric acids, then catalytically hydrogenate the intermediate. But you're not going to do it at all if you can't raise the intermediate to 300 degrees C.
Aniline is the name of benzene with an NH2 group attached.
Partially true because benzene also obtained from other sources.
The chemical fomula of aniline is C6H7N.
aniline is more acidic because in aniline a electron withdrawing benzene is connected.electron withdrawing capacity of benzene is due to its delocalizing pi electrons cloud.due the action of benzene the presence of unshared pair of electron over nitrogen is somehow decreases.which increases its acidic nature. But in case of ammonia there is no electron withdrawing group.so its unshared pair of electron remains undistrubed,which decreases its acidity and increases its basisity
Some examples of organic compounds that contain the benzene ring are benzene itself, toluene, phenol, aniline, and styrene. These compounds are aromatic hydrocarbons that share the characteristic hexagonal structure of the benzene ring.
Aniline is the name of benzene with an NH2 group attached.
Partially true because benzene also obtained from other sources.
The chemical fomula of aniline is C6H7N.
With hydrogen in a catalized reaction
aniline is more acidic because in aniline a electron withdrawing benzene is connected.electron withdrawing capacity of benzene is due to its delocalizing pi electrons cloud.due the action of benzene the presence of unshared pair of electron over nitrogen is somehow decreases.which increases its acidic nature. But in case of ammonia there is no electron withdrawing group.so its unshared pair of electron remains undistrubed,which decreases its acidity and increases its basisity
The product obtained by bromination of aniline using bromine is 2,4,6-tribromoaniline. This reaction involves the substitution of hydrogen atoms on the benzene ring of aniline with bromine atoms.
Some examples of organic compounds that contain the benzene ring are benzene itself, toluene, phenol, aniline, and styrene. These compounds are aromatic hydrocarbons that share the characteristic hexagonal structure of the benzene ring.
The isomeric amines of formula C7H9N that contain a benzene ring are aniline and 2-aminotoluene. Aniline has the formula C6H5NH2, while 2-aminotoluene has the formula C7H7NH2.
Use acetic anhydride as reagent. The reaction will undergo nucleophilic addition and the reagent will attach to the amine group. Half of the reagent will become the leaving group and one H of the amine group in the reactant will leave with the reagent. The product will be the benzene ring with an amine, carbonyl, methyl attached.
Aniline is an unsaturated compound as it contains a benzene ring, which is a form of unsaturation due to the delocalized pi electron system.
You can convert aniline to chlorobenzene by reacting it with chlorine in the presence of a Lewis acid catalyst such as iron (III) chloride (FeCl3). The reaction proceeds via electrophilic aromatic substitution to replace the amino group with a chlorine atom on the benzene ring to form chlorobenzene.
The product of a reaction between bromine and aniline in a non-polar solvent is typically the bromination of aniline, where bromine substitutes a hydrogen atom on the benzene ring of aniline to form bromoaniline. This reaction is an electrophilic aromatic substitution reaction.