AlCl3 will take Cl out from CH3COCl which becomes CH3CO+. CH3CO+ is an electrophillic thus attracting to the negative ring of benzene. To form a ketone-Phenylethanone. CH3COCl + AlCl3 = CH3CO+ and AlCl4- . C6H6 + CH3CO+ = C6H5COCH3 + HCL.
This is an example of a Friedel-Crafts acylation. One hydrogen from the benzene is replaced by the acetyl portion of the acetyl chloride and the hydrogen and chloride from the benzene and acetyl chloride respectively combine to form HCl. Please see the link.
bum
The substitution reactions of phenol are easier than benzene, phenol directly reacts with bromine and gives tribromo phenol while benzene requires FeCl3 as a catalyst and gives mono bromo phenol.
35g C6H6* 1mol C6H6/78.108g C6H6 * 1 mol C6H5Br/ 1 mol C6H6 * 157g C6H5Br/1mol C6H5Br = 70.35g of Bromobrezene.
It exothermically reacts and dissolves
This is an example of a Friedel-Crafts acylation. One hydrogen from the benzene is replaced by the acetyl portion of the acetyl chloride and the hydrogen and chloride from the benzene and acetyl chloride respectively combine to form HCl. Please see the link.
bum
No, it does not
it gets converted into gemmaxane c6cl6
No!! Benzene wont de colourise bromine water although it is an unsaturated compound ,as it is an aromatic compound and it does not undergo addition reaction.
The substitution reactions of phenol are easier than benzene, phenol directly reacts with bromine and gives tribromo phenol while benzene requires FeCl3 as a catalyst and gives mono bromo phenol.
BENZENE Formula C6H6Reaction with Ozone C6H6 + 11 O3 ---- > 6C02 + 3 H2O + 11 O2 Number of O2 molecules consumed per molecule of compound = 5.5
Aluminum sulfate Al2(SO4)3 will form when aluminum reacts with sulfur in the presence of oxygen.
Salt
Benedict's solution reacts to the presence of monosaccrhrides
35g C6H6* 1mol C6H6/78.108g C6H6 * 1 mol C6H5Br/ 1 mol C6H6 * 157g C6H5Br/1mol C6H5Br = 70.35g of Bromobrezene.
al2o3