Chemguide: Support for CIE A level Chemistry Learning outcome 10.5(b) This statement is about the mechanism for the reaction between hydrogen cyanide and aldehydes or ketones. Before you go on, you should find and read the statement in your copy of the syllabus. Sorting out statement 10.5(b) You will find this on the page about the mechanism for the reactions between carbonyl compounds and hydrogen cyanide. You will probably want to follow the link to the "Talk me through . . ." page as well. CIE want a simplified version of all this, and so there are bits of those pages which you can ignore, or just skim through quickly if you are interested. You will be asked about this mechanism using hydrogen cyanide in the presence of some cyanide ions. You do not need to worry about exactly how this is achieved, or the reasons for the pH chosen for the reaction. Just learn that you use HCN together with some cyanide ions (from, say, sodium cyanide) as a catalyst. You will not be asked about the optical isomerism parts of these pages - ignore them. However, you must show the second stage of the mechanism properly as a reaction between the intermediate ion and an HCN molecule regenerating the cyanide ion catalyst. A common follow-on from questions involving this statement Quite a lot of questions follow this up by looking at the hydrolysis of the -CN group in the product molecule to give a carboxylic acid. This is dealt with in statement 10.6(a). Bear this in mind when you come to do your revision.
© Jim Clark 2011 (modified August 2013) |