**Part
6: THERMODYNAMICS**

This should have been a reasonably straight forward calculation, but care needs to be taken with the last part of the question.

**a. ** C

**b. ** DHc **elements** = (5 x -94.05) + (6 x -68.32) = -880.17 kcal/mol (0.5 marks)

DHf** X**= -880.17 - (- 840.03) = -40.14 kcal/mol (0.5 marks)

DHc **Y** = -880.17 - (- 36.73) = -843.44 kcal/mol (0.5 marks)

**c**. (1.5 marks)

**d.**

** **

**e**.Given the thermodynamic data in the table provided in the question, and hence the figure shown above, **X **is the most stable isomer (*i.e*. lowest energy) and **Z** is the least stable isomer (1 mark)

**f.** The more branched isomer is more stable because branching increases the number of primary C atoms and hence the number of primary C-H bonds. Since, in terms of bond strength, primary C-H bonds > secondary C-H > tertiary C-H, a molecule with more primary C-H (more branching) is more stable (1 mark)

**g. **Since the radical chlorination reaction gives 3 mono-chlorination products, the starting material must have had 3 types of H and hence the starting material is pentane, isomer **Z **(**X** has 1 type and **Y** has 4 types). The major product of mono-chlorination of pentane is 2-chloropentane (which we can confirm by considering the relative yields based on the terms from the equation that predicts the yields of these reactions.

**Common errors**:

- incorrect coefficients in the balanced equation
- missing signs in calculated values
- incorrect or no labelling of the most and least stable isomers based on the thermodynamic numbers. X is the most stable because it is at the lowest energy (see the figure).
- drawing an isomer of
C_{5}H_{12}that did not fit the required molecular formula or was the same as one already drawn - not matching X, Y and Z to the correct structure
- incomplete or vague explanation based on bonding of why a more branched isomer is more stable. Typically students did not talk about the strengths of the bonds involved which is the key part.
- incorrect analysis of the radical chlorination reaction information