$2.4 \ g$ coal is burnt in a bomb calorimeter in excess of oxygen at $298 \ K$ and $1 \ atm$ pressure. The temperature of the calorimeter rises from $298 \ K$ to $300 \ K$. The enthalpy change during the combustion of coal is $-x \ kJ \ mol^{-1}$. The value of $x$ is. (Nearest Integer) (Given: Heat capacity of bomb calorimeter $20.0 \ kJ \ K^{-1}$. Assume coal to be pure carbon)

  • A
    $201$
  • B
    $202$
  • C
    $203$
  • D
    $200$

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Match the following terms in Column-$I$ with their corresponding descriptions in Column-$II$:
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$(b)$ Isolated system$(2)$ At constant volume
$(c)$ Isothermal change$(3)$ First law of thermodynamics
$(d)$ Path function$(4)$ No exchange of matter and energy
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$(g)$ Law of conservation of energy$(7)$ Internal energy
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Enthalpy of formation of $CO_{2(g)}$,$H_2O_{(l)}$ and $C_6H_{12}O_{6(s)}$ are $-393$,$-286$ and $-1170 \ kJ \ mol^{-1}$ respectively. The quantity of heat liberated when $18 \ g$ of $C_6H_{12}O_{6(s)}$ is burnt completely in oxygen is (in $kJ$)

$\Delta H_f^o$ of water is $-285.5\, kJ\, mol^{-1}$. If enthalpy of neutralisation of monoacidic strong base is $-57.3\, kJ\, mol^{-1}$,$\Delta H_f^o$ of $OH^{-}$ ion will be $.....\, kJ\, mol^{-1}$.

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