Benzoyl chloride is C6H5COCI and benzyl chloride is C6H5CH3CI
benzoylisothiocyanate
1.21g
Yes. KCl will dissolve in ethanol.
reacting a benzoyl chloride with a phenol to get an phenyl benzoate(ester).
Benzoyl chloride is C6H5COCI and benzyl chloride is C6H5CH3CI
bcos there s a strong resonance n benzoyl chloride so that can't easily loose electrons..........
benzanilide
it has 2 benzene rings usually synthesized in the lab from benzoyl chloride and hydrogen peroxide
benzoylisothiocyanate
1.21g
The benzyl group acts as a protector retarding hydrolysis?
Sodium chloride is an ionic compound and ethanol has only a weak polarity.
I dont think it does :)xx ----------------------------------- The solubility of sodium chloride in ethanol is very low: 0,65 g/L at 25 0C.
Yes. KCl will dissolve in ethanol.
Remember that acid chlorides typically undergo nucleophilic substitution in which the partially positively charged carbon is attacked by nucleophile. Due to resonance(delocalization) in benzoyl chloride, the positive charge isn't concentrated in carbonyl C atom unlike in ethanoyl chloride but spreads over o and p positions in benzene ring. So, the carbonyl carbon in benzoyl chloride is less positive, less susceptible to nucleophilic attack and hence, less reactive.
Metallic sodium reacts vigorously with ethanol to form sodium ethanoate.