Draw the mechanism for the reaction between ethanoyl chloride and a nucleophile

nucleophile will attack partially postive charged carbon, and kick out leaving group i.e the chloride ion. Giving a product.

JT

Related Chemistry A Level answers

All answers ▸

Predict the relative boiling points of propanal, butane and prop-2-en-1-ol from the highest to the lowest boiling point


Why do first ionisation energies decrease down a group but increase across a period?


Part a) Draw the mechanism of the attack of CN- on CH3COCH3 in the presence of HCN Part b) Explain why the product of this reaction does not rotate the plane of plane polarised light


Predict the boiling points (lowest to highest) of Butan-1-ol, 2-methylpropane and Butane