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 ▸Rank the following acids according to acid strength, strongest to weakest: HF, HCl, HBr. Explain your reasoning.
What is the trend in electronegativity of group 7?
How would you test for the presence of a phenol?
What is bond polarity and why does it exist?