Q.The amount of heat exchanged with the surrounding at constant pressure is given by the quantity

Enthalpy, $H=U+PV$, is a state function reflecting a system's capacity to do mechanical work and release heat. Its central usefulness: at CONSTANT PRESSURE, the heat involved in a process exactly equals its change in enthalpy, $\Delta H=q_p$. So $\Delta H$ positive signals an endothermic process (heat absorbed), $\Delta H$ negative signals exothermic (heat released) -- a sign convention used everywhere else in the chapter.

Deriving the relation to internal energy: applying $H=U+PV$ to an initial and final state at constant pressure and subtracting gives $\Delta H=\Delta U+P\Delta V$; substituting the first law ($\Delta U=q+w$, $w=-P\Delta V$) confirms $\Delta H=q_p$ directly. For a gas-phase reaction specifically, applying the ideal gas law to reactant and product gas volumes separately and subtracting gives $P\Delta V=\Delta n_{(g)}RT$, so the chemist's working formula is

where $\Delta n_{(g)}$ = moles of gaseous products minus moles of gaseous reactants (solids/liquids don't count). This single equation is the standard bridge between a bomb calorimeter's constant-volume measurement ($\Delta U$) and the constant-pressure enthalpy ($\Delta H$) that chemists actually want to quote and compare.