| A | B |
|---|
| CH3.CO.Cl is called | ethanoyl chloride |
| CH3.CH2.CO.Cl is called | prpanoyl chloride |
| CH3.CH2.CH2.CO.Cl is called | butanoyl chloride |
| when a bottle of CH3.CO.Cl is opened white acidic fumes are observed these are.. | hydrogen chloride |
| CH3.CO.Cl + H2O products | CH3.CO.OH + HCl |
| CH3.CO.Cl + NH3 products | CH3.CO.NH2 + Cl |
| CH3.CO.OH is called | ethanoic acid |
| CH3.CO.NH2 is called | ethanamide |
| CH3.CO.Cl + H2O or NH3 reaction type is | nucleophilic substitution |
| H2O or NH3 are nucleophiles because they | seek a (+) centre on the CH3.CO.Cl molecule |
| CH3.CO.Cl reacts more vigorously with H2O than CH3Cl because | a higher (+) charge induced in C of the CO by electron attraction of the O atom |
| CH3.CO.Cl + C2H5NH2 products | CH3.CO.NH.C2H5 + HCl |
| CH3.CO.NH.C2H5 is called | N-ethyl ethanamide |
| CH3.CO.Cl + C6H5NH2 products | CH3.CO.NH.C6H5 + HCl |
| C6H5NH2 is called | phenylamine (or aniline) |
| CH3.CO.NH.C6H5 is called | N-phenyl ethanamide |
| CH3.CO.Cl + C2H5OH products | CH3.CO.OC2H5 + HCl |
| CH3.CO.OC2H5 is called | ethyl ethanoate |
| CH3.CO.Cl + C2H5OH gives a better yield than CH3COOH & C2H5OH because | it is not a reversible reaction |
| CH3.CH2.CO.NH.C2H5 reactants | CH3.CH2.CO.Cl & C2H5.NH2 |
| CH3.CH2.CH2.CO.OC2H5 reactants | CH3.CH2.CH2.CO.Cl & C2H5OH |
| CH3.CH2.CH2.CO.OC2H5 is called | ethyl butanoate |
| CH3.CH2.CO.NH.C2H5 called | N-ethyl propanamide |
| CH3.CO.Cl + CH3.CH2.CH2OH products | CH3.CO.O CH2.CH2.CH3 + HCl |
| CH3.CO.O CH2.CH2.CH3 is called | propyl ethanoate |
