m/j 07
q5 c, cyanide has a triple bond so 3 bonding pairs. Nitrogen shares 3 electrons leaving 2 forming one lone pair. Carbon has a charge of -1 in cyanide so it has an extra electron. it shares 3 electrons and leaves two again forming one lone pair
q26 c, it cannot react with acidified manganate(VII) ions so it has to be a tertiary alcohol. the simplest tertiary alcohol is butanol but its is not chiral, next is pentanol again not chiral and has no chiral isomers neither does hexanol, but a 7 carbon alcohol (2-methylhexan-2-ol) is chiral since the central carbon is bonded to four different groups, CH3, C2H5, and C3H7 ( try drawing it to visualize it better)
q28 c, it decolourises 2,4-DNPH so it must be a ketone or an aldehyde but it also de-colourises manganate(VII) ions so it must be able to be oxidised. ketones cannot be oxidised further, but aldehydes can so C
q40 D, 1 only, heating an easter with an acid will hydrolysithe ester bond and therefore break it. alcohol or sodium hydrogen-carbonate will have no effect the ester bond.