Well that clears all the confusion guys. Primary Amides undergo base hydrolysis to form a carboxylic acid salt, primary amides also undergo acid hydrolysis to form a carboxylic acid and an ammonium salt. The reason why it stated that amides undergo base hydrolysis in the june 2013 question was because the question was referring to peptide linkages and the amide/peptide bond is a secondary amide. When you hydrolyse a peptide bond you form a carboxylic acid and an amine, it's exactly how two amino acids are seperated using hydrolysis.
EDIT: Actually I'd say it was pretty difficult, I reckon there'll be lower grade boundaries for that - certainly lower than last summer's which was literally 90% for an A*! I wouldn't worry too much if you found it diffuclt!
The compound W alkene questions were rather funny, I can see them throwing some people off. The first part of section B was also difficult IMO, and the for the 1 marker on the last page, what is missing from the first bullet point, what did you guys write?
The compound W alkene questions were rather funny, I can see them throwing some people off. The first part of section B was also difficult IMO, and the for the 1 marker on the last page, what is missing from the first bullet point, what did you guys write?
Completely agree, start of question 4 was pretty hard! Had no idea what was missing from the first bullet point, I must have stared at it for a good 2 minutes hahah
The compound W alkene questions were rather funny, I can see them throwing some people off. The first part of section B was also difficult IMO, and the for the 1 marker on the last page, what is missing from the first bullet point, what did you guys write?