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Why is it that aniline has a high boiling point to phenol and phenol has a high boiling point than toluene and toluene has a high boiling point than benzene?
Aniline has a higher boiling point than phenol because aniline can form strong hydrogen bonds due to the presence of an amino group. Phenol has a higher boiling point than toluene because phenol molecules can form intermolecular hydrogen bonds because of the hydroxyl group. Toluene has a higher boiling point than benzene due to the presence of a bulky methyl group which increases Van der Waals forces between toluene molecules.
Toluene (C7H8) is one of the components of crude oil. Which shows the balanced combustion reaction for toluene?
it,s C7H8+9O2>7CO2+4H2O+HEATapexx
Acidified potassium permanganate reaction with toluene equation?
The reaction between acidified potassium permanganate and toluene results in the oxidation of toluene to benzoic acid. The balanced chemical equation for this reaction is: C7H8 + 2KMnO4 + 8H2SO4 → 2MnSO4 + K2SO4 + 7H2O + 7H2O + C6H5CO2H
What happens when chlorine is passed through boiling toluene?
Electrophilic halogenation
What results will you get if you add bromine in toluene?
When bromine is added to toluene, bromination of the aromatic ring can occur. This reaction can lead to the formation of mono- or poly-brominated toluene derivatives, depending on reaction conditions. Products may include ortho-, meta-, or para-bromotoluene isomers.
How do you convert toluene to aniline?
To convert toluene to aniline, you can first nitrify toluene to form nitrotoluene using a mixture of concentrated nitric and sulfuric acids. Then, the nitrotoluene can be reduced to aniline through catalytic hydrogenation or using reducing agents like iron and hydrochloric acid or lithium aluminum hydride. This process involves the substitution of the nitro group with an amino group, resulting in the formation of aniline.
How do you write the nucleophilic substitution reactions for aniline and toluene?
aniline would go through an electrophilic substitution, it is a weak base
Why is it that aniline has a high boiling point to phenol and phenol has a high boiling point than toluene and toluene has a high boiling point than benzene?
Aniline has a higher boiling point than phenol because aniline can form strong hydrogen bonds due to the presence of an amino group. Phenol has a higher boiling point than toluene because phenol molecules can form intermolecular hydrogen bonds because of the hydroxyl group. Toluene has a higher boiling point than benzene due to the presence of a bulky methyl group which increases Van der Waals forces between toluene molecules.
Products of the reaction between bromine and toluene?
The reaction between bromine and toluene can result in the substitution of a hydrogen atom on the toluene ring with a bromine atom, forming bromotoluene. Different isomers of bromotoluene can be produced depending on the position of the bromine atom on the toluene ring.
What are the products of a toluene sulfuric acid reaction?
para-toluene sulfonic acid and ortho toluene sulfonic acid p-CH3-C6H4-SO3H and o-CH3-C6H4-SO3H
Toluene (C7H8) is one of the components of crude oil. Which shows the balanced combustion reaction for toluene?
it,s C7H8+9O2>7CO2+4H2O+HEATapexx
Acidified potassium permanganate reaction with toluene equation?
The reaction between acidified potassium permanganate and toluene results in the oxidation of toluene to benzoic acid. The balanced chemical equation for this reaction is: C7H8 + 2KMnO4 + 8H2SO4 → 2MnSO4 + K2SO4 + 7H2O + 7H2O + C6H5CO2H
What happens when chlorine is passed through boiling toluene?
Electrophilic halogenation
What is the product of cyclohexane and toluene?
there is no chemical reaction between these two.
What results will you get if you add bromine in toluene?
When bromine is added to toluene, bromination of the aromatic ring can occur. This reaction can lead to the formation of mono- or poly-brominated toluene derivatives, depending on reaction conditions. Products may include ortho-, meta-, or para-bromotoluene isomers.
What happens when excess Chlorine is passed through boiling toluene?
When excess chlorine is passed through boiling toluene, chlorination of the toluene molecule can occur. This reaction can lead to the introduction of chlorine atoms into the benzene ring of toluene, resulting in the formation of chlorinated derivatives of toluene. These derivatives can have different properties and reactivity compared to the original toluene molecule.
What happens when Toluene reacts with Chlorine in presence of sun light?
When toluene reacts with chlorine in the presence of sunlight, a substitution reaction occurs where one or more hydrogen atoms in the toluene molecule are replaced by chlorine atoms. This reaction can result in the formation of different chlorinated derivatives of toluene, such as benzyl chloride or benzal chloride, depending on the conditions and the position of the substitution on the benzene ring.
