recall the reactions (reagents and conditions) by which aldehydes and ketones can be produced: (a) the oxidation of primary alcohols using acidified \( K_2Cr_2O_7 \) or acidified \( KMnO_4 \) and distillation to produce aldehydes (b) the oxidation of secondary alcohols using acidified \( K_2Cr_2O_7 \) or acidified \( KMnO_4 \) and distillation to produce ketones

describe: (a) the reaction with oxygen (combustion) (b) substitution to form halogenoalkanes, e.g. by reaction with HX(g); or with KCl and concentrated \( H_2SO_4 \) or concentrated \( H_3PO_4 \); or with PCl\(_3\) and heat; or with PCl\(_5\); or with SOCI\(_2\) (c) the reaction with Na(s) (d) oxidation with acidified \( K_2Cr_2O_7 \) or acidified KMnO\(_4\) to: (i) carbonyl compounds by distillation (ii) carboxylic acids by refluxing (primary alcohols give aldehydes which can be further oxidised to carboxylic acids, secondary alcohols give ketones, tertiary alcohols cannot be oxidised) (e) dehydration to an alkene, by using a heated catalyst, e.g. \( Al_2O_3 \) or a concentrated acid (f) formation of esters by reaction with carboxylic acids and concentrated \( H_2SO_4 \) as catalyst as exemplified by ethanol

describe the following reactions of alkenes: (a) the electrophilic addition of (i) hydrogen in a hydrogenation reaction, \( H_2(g) \) and Pt/Ni catalyst and heat (ii) steam, \( H_2O(g) \) and \( H_3PO_4 \) catalyst (iii) a hydrogen halide, \( HX(g) \), at room temperature (iv) a halogen, \( X_2 \) (b) the oxidation by cold dilute acidified \( KMnO_4 \) to form the diol (c) the oxidation by hot concentrated acidified \( KMnO_4 \) leading to the rupture of the carbon–carbon double bond and the identities of the subsequent products to determine the position of alkene linkages in larger molecules (d) addition polymerisation exemplified by the reactions of ethene and propene