Answers>Chemistry>A Level>Article

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

Answered by Jake T. • Chemistry tutor

3228 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Carbon dioxide is a gas at room temperature while silicon dioxide is a solid at room temperature with a melting point of 1770°C. Explain this by comparing their particles and those forces between these particles.

How does free radical substitution work?

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

Explain the trend in melting points of the period 3 elements