(a)[1]
Complete Table 6.1 so that it shows how many $\mathrm{sp}$, $\mathrm{sp^2}$ and $\mathrm{sp^3}$ hybridised carbon atoms are present in one molecule of Z.
(b(i))[1]
Z is able to undergo several reactions, as illustrated in Fig. 6.1. Name the two reaction types taking place in reaction 7 in Fig. 6.1.
(b(ii))[4]
Draw the structures for the organic products from reactions 7, 8 and 9 in Fig. 6.1.
(c(i))[1]
Predict how many peaks appear in the carbon-13 NMR spectrum of Z.
(c(ii))[2]
The proton ($^1$H) NMR spectrum of Z in D$_2$O shows three peaks for the proton environments, labelled a, b and c, as illustrated in Fig. 6.2. Complete Table 6.2 for the proton ($^1$H) NMR spectrum of Z in D$_2$O.