bcos there s a strong resonance n benzoyl chloride so that can't easily loose electrons..........
The benzyl group acts as a protector retarding hydrolysis?
Ten nonbonding electrons and 14 bonding electrons are in acetyl chloride.
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.
It would most likely react by backside attack to form methyl chloride.
acetic anhydride and sodium chloride will form.
The benzyl group acts as a protector retarding hydrolysis?
4-acetyl biphenyl
Ten nonbonding electrons and 14 bonding electrons are in acetyl chloride.
Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid
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.
The nucleophilic nitrogen attacks the carbonyl carbon of acetyl chloride. HCl gas is released and acetyl glycine is formed.
i do not have the answer
It would most likely react by backside attack to form methyl chloride.
acetic anhydride and sodium chloride will form.
Albert Iven Ezell has written: 'Preparation and properties of the acetyl, benzoyl and methyl derivatives of soda lignin' -- subject(s): Lignin
The chemical name for CH3CO2Cl is acetyl chloride.
The mass is 4,178 kg (for the US gallon).