Freidel Craft Alkylation Acylation
Trending Questions
Q.
How would you convert the following compounds into benzene?
(i) Ethyne
(ii) Ethene
(iii) Hexane
Q. Friedel-Crafts alkylation is expected to proceed through a carbocation intermediate. What would be the alkylation product when benzene reacts with cyclopropyl chloride in the presence of AlCl3?
Q.
How will you prepare the following compounds from benzene ? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
Methyl benzoate
m - nitrobenzoic acid
p - nitrobenzoic acid
Phenyl acetic acid
p - nitrobenzaldehyde.
Q.
What happens when phenol is treated with bromine?
Q.
Arrange the following: in order of increasing acidity
Q.
How will you convert Benzene to Benzoic acid?
Q. Benzene reacts with n-propyl chloride in the presence of anhydrous AlCl3 to give predominantly
- 3-propyl-1-chlorobenzene
- no reaction
- n-propyl benzene
- isopropyl benzene
Q.
Complete the following reaction:-
Q. Compound “A” on reduction with Sn/HCl gives “B” which on further reaction with CHCl3 and alcoholic KOH gives compound “C”. The compound upon hydrolysis gives aniline. The compound “A” is :
- nitrobenzene
- methylamine
- nitromethane
- nitrosobenzene
Q.
Which of the following compound would undergo SN1 reaction faster and why?
(C6H5)CH2Cl. Or. (C6H11)CH2Cl
Q. Which of the following compound will undergo electrophilic substitution more readily than benzene?
- Nitrobenzene
- Benzoic acid
- Benzaldehyde
- Phenol
Q. For preparing monoalkyl benzene, acylation process is preferred than direct alkylation because:
- in alkylation, a poisonous gas is evolved
- in alkylation, large amount of heat is evolved
- in alkylation, polyalkylated product is formed
- alkylation is very costly
Q. Predict the major product in the following reaction :
Q.
How would you convert the following compounds into benzene?
(i) Ethyne (ii) Ethene (iii) Hexane