The heat of neutralization of a weak acid and a strong base is less than the heat of neutralization of a strong acid and a strong base due to:

From the given data at $298 \, K$:
$\Delta H_f^o [CO_2, g] = -394 \, kJ/mol$
$\Delta H_f^o [H_2O, l] = -286 \, kJ/mol$
$\Delta H_f^o [propene, g] = 20 \, kJ/mol$
$cyclopropane (g) \to propene (g)$; $\Delta H^o_{isomerisation} = -33 \, kJ/mol$.
Calculate $\Delta H^o_{combustion} [cyclopropane, g]$.
$...... \, kJ/mol$

What will be the $C-H$ bond enthalpy if:
$CH_{4(g)} + 2O_{2(g)} \rightarrow CO_{2(g)} + 2H_2O_{(l)};$ $\Delta H = -890 \, kJ$
$CO_{2(g)} \rightarrow C_{(graphite)} + O_{2(g)};$ $\Delta H = 393 \, kJ$
$2H_2O_{(l)} \rightarrow 2H_{2(g)} + O_{2(g)};$ $\Delta H = 571 \, kJ$
$2H_{2(g)} \rightarrow 4H_{(g)};$ $\Delta H = 871 \, kJ$
$C_{(graphite)} \rightarrow C_{(g)};$ $\Delta H = 716 \, kJ$

If the standard enthalpies of formation of hydrazine and water are $+50.6 \, kJ/mol$ and $-285.9 \, kJ/mol$ respectively,calculate the $\Delta H$ for the following reaction: $N_2H_{4(g)} + O_{2(g)} \to N_{2(g)} + 2H_2O_{(l)}$ in $kJ \, mol^{-1}$.

When $4 \ g$ of iron is burnt to ferric oxide at constant pressure,$29.28 \ kJ$ of heat is evolved. What is the enthalpy of formation of ferric oxide in $kJ \ mol^{-1}$? (At. Wt. of $Fe = 56$)

For the following reaction,
$C (diamond) + O_2 \rightarrow CO_{2(g)}$; $\Delta H = -97.6 \ kcal$
$C (graphite) + O_2 \rightarrow CO_{2(g)}$; $\Delta H = -94.3 \ kcal$
The heat change for the conversion of $1 \ g$ of $C (diamond) \rightarrow C (graphite)$ is (in $kcal$)