What is the molar heat of combustion when #"25000 g"# of methanol is combusted in a bomb calorimeter to raise the temperature of the surrounding water by #40^@ "C"# if the heat capacity of the calorimeter is #"10.4 kJ/"^@ "C"#?
1 Answer
There's probably an error in this question... I get
Since we are in a bomb calorimeter, a constant-volume calorimeter, we have from the first law of thermodynamics:
#q_V = DeltaU + cancel(PDeltaV)^(0)# ,where:
#q_V# is the heat flow at constant volume.#DeltaU# is the change in internal energy.- The work done,
#-PDeltaV# , is defined here as the system doing work with respect to the surroundings.
Since we know the change in temperature and the combined heat capacity (presumably in
#|q_V| = C_VDeltaT#
#= "10.4 kJ/"^@ "C" xx 40^@ "C"#
#=# #"416 kJ"#
I interpret the molar heat of combustion to be
#DeltabarU_C = q_V/n_(LR)# ,where
#n_(LR)# is the mols of the limiting reactant, i.e. the methanol in the presence of oxygen.
Assuming complete combustion:
#2"CH"_3"OH"(g) + 3"O"_2(g) -> 4"H"_2"O"(g) + 2"CO"_2(g)#
The molar internal energy of combustion is then the heat released out from the reaction towards the surrounding water:
#color(blue)(DeltabarU_C) = -("416 kJ")/(25000 cancel("g CH"_3"OH")) xx (32.04 cancel("g CH"_3"OH"))/"1 mol"#
#=# #color(blue)(-"0.5331 kJ/mol")#
This is an absurdly low number, so there's something off with the data... Are you sure it isn't