Based on the bond enthalpy $(B.E.)$ values given,the standard enthalpy of formation $(\Delta_fH^o)$ of $N_2H_{4(g)}$ is ...... $kJ\ mol^{-1}$.
Given: $B.E.(N-N) = 159\ kJ\ mol^{-1}$,$B.E.(H-H) = 436\ kJ\ mol^{-1}$,$B.E.(N \equiv N) = 941\ kJ\ mol^{-1}$,$B.E.(N-H) = 398\ kJ\ mol^{-1}$.

  • A
    $711$
  • B
    $62$
  • C
    $-98$
  • D
    $-711$

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The enthalpy changes for the following processes are listed below:
$Cl_{2(g)} \to 2Cl_{(g)}$,$\Delta H = 242.3 \ kJ \ mol^{-1}$
$I_{2(g)} \to 2I_{(g)}$,$\Delta H = 151.0 \ kJ \ mol^{-1}$
$ICl_{(g)} \to I_{(g)} + Cl_{(g)}$,$\Delta H = 211.3 \ kJ \ mol^{-1}$
$I_{2(s)} \to I_{2(g)}$,$\Delta H = 62.76 \ kJ \ mol^{-1}$
Given that the standard states for iodine and chlorine are $I_{2(s)}$ and $Cl_{2(g)}$,the standard enthalpy of formation for $ICl_{(g)}$ is .............. $kJ \ mol^{-1}$

Consider the following reactions:
$(i)$ $H_{(aq)}^{+} + OH^{-}_{(aq)} \longrightarrow H_2O_{(l)}$,$\Delta H = -X_1 \ kJ \ mol^{-1}$
$(ii)$ $H_{2_{(g)}} + \frac{1}{2} O_{2_{(g)}} \longrightarrow H_2O_{(l)}$,$\Delta H = -X_2 \ kJ \ mol^{-1}$
$(iii)$ $CO_{2_{(g)}} + H_{2_{(g)}} \longrightarrow CO_{(g)} + H_2O_{(l)}$,$\Delta H = -X_3 \ kJ \ mol^{-1}$
$(iv)$ $C_2H_{2_{(g)}} + \frac{5}{2} O_{2_{(g)}} \longrightarrow 2CO_{2_{(g)}} + H_2O_{(l)}$,$\Delta H = -X_4 \ kJ \ mol^{-1}$
Enthalpy of formation of $H_2O_{(l)}$ is

The lowest value of heat of neutralization is obtained for

Given: $S + \frac{3}{2} O_2 \to SO_3 + 2x \ \text{kcal}$,$\Delta H = -2x \ \text{kcal}$ and $SO_2 + \frac{1}{2} O_2 \to SO_3 + y \ \text{kcal}$,$\Delta H = -y \ \text{kcal}$. Find the heat of formation of $SO_2$.

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Consider the reaction $4NO_2(g) + O_2(g) \rightarrow 2N_2O_5(g)$, $\Delta_rH = -111 \ kJ$. If $N_2O_5(s)$ is formed instead of $N_2O_5(g)$, what will be the value of $\Delta_rH$ in $kJ$? (Given: $\Delta H_{sub} = 54 \ kJ \ mol^{-1}$ for $N_2O_5$)

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