Which of the following is not correct?
1. is zero for a reversible reaction.
2. is positive for a spontaneous reaction.
3. is negative for a spontaneous reaction.
4. is positive for a non-spontaneous reaction.
A necessary condition for an adiabatic change is-
1. ∆T = 0
2. ∆P = 0
3. q = 0
4. w = 0
The enthalpy of formation of all elements in their standard state is-
1. | Unity | 2. | Zero |
3. | Less than zero | 4. | Different for each element |
for combustion of methane is –x kJ mol–1.
The value of for the same reaction would be:
701 J of heat is absorbed by a system and 394 J of work is done by the system. The change in internal energy for the process is-
1. | 307 J | 2. | -307 J |
3. | 1095 J | 4. | -701 J |
The reaction of cyanamide, with dioxygen, was carried out in a bomb calorimeter, and ∆U was found to be at 298 K.
\(\small{\mathrm{NH}_2 \mathrm{CN}(\mathrm{s})+\frac{3}{2} \mathrm{O}_2(\mathrm{g}) \rightarrow \mathrm{N}_2(\mathrm{g})+\mathrm{CO}_2(\mathrm{g})+\mathrm{H}_2 \mathrm{O}(\mathrm{l})}\)
The enthalpy change for the reaction at 298 K would be -
The amount of heat needed to raise the temperature of 60.0 g of aluminium from 35°C to 55°C would be -
(Molar heat capacity of Al is )
The enthalpy of formation of are
–110 kJ , – 393 kJ , 81 kJ and 9.7 kJ respectively.
The value of for the reaction would be-
. The standard enthalpy of formation of gas in the above reaction would be-
1. | -92.4 J (mol)-1 | 2. | -46.2 kJ (mol)-1 |
3. | +46.2 J (mol)-1 | 4. | +92.4 kJ (mol)-1 |
The standard enthalpy of the formation of CH3OH(l) from the following data is:
\(\small{\mathrm{CH}_3 \mathrm{OH}_{(l)}+\frac{3}{2} \mathrm{O}_2(\mathrm{g}) \rightarrow \mathrm{CO}_2(\mathrm{g})+2 \mathrm{H}_2 \mathrm{O}_{(l)} \text {; }}\) \( \Delta_{\mathrm{r}} \mathrm{H}^{\circ}=-726 \mathrm{~kJ} \mathrm{~mol}{ }^{-1}\) |
\(\small{\mathrm{C}(\mathrm{s})+\mathrm{O}_2(\mathrm{g}) \rightarrow \mathrm{CO}_2(\mathrm{g}) \text {; } }\) \(\Delta_{\mathrm{c}} \mathrm{H}^{\circ}=-393 \mathrm{~kJ} \mathrm{~mol}{ }^{-1}\) |
\(\small{\mathrm{H}_{2(\mathrm{g})}+\frac{1}{2} \mathrm{O}_{2(\mathrm{g})} \rightarrow \mathrm{H}_2 \mathrm{O}_{(l)} \text {; } } \) \(\Delta_{\mathrm{f}} \mathrm{H}^{\circ}=-286 \mathrm{~kJ} \mathrm{~mol}^{-1}\) |
1. | −239 kJ mol−1 | 2. | +239 kJ mol−1 |
3. | −47 kJ mol−1 | 4. | +47 kJ mol−1 |