Chemistry 9701/23 — May/June 2017
Cambridge AS Level · AS Level Structured Questions · worked solutions for every part, with the mark scheme
Topics Introduction to Organic Chemistry · Hydrocarbons · Atoms, Molecules and Stoichiometry · States of Matter · Group 17 · Electrochemistry · +3 more
Combustion data can be used to calculate the empirical formula, molecular formula and relative molecular mass of many organic compounds. Combustion data cannot distinguish between different structural isomers.
Define the term structural isomers.
is a hydrocarbon, . A gaseous sample of occupied a volume of at and .
The sample was completely burned in of oxygen (an excess).
The final volume, measured under the same conditions as the gaseous sample (so that the water produced is liquid and its volume can be ignored), was .
Treating the remaining gaseous mixture with concentrated alkali, to absorb carbon dioxide, decreased the volume to .
The equation for the complete combustion of can be represented as shown.
Use the data given to calculate the value of .
Use the data given to calculate the value of .
If you were unable to calculate values in (b)(i) and (b)(ii) then use the data in this box for the remaining parts of this question. These are not the correct values.
Give the molecular formula and the empirical formula of .
is unbranched.
Give the skeletal formulae for two possible structures of that are positional isomers of each other.
Use the general gas equation to calculate the mass of present in the original gaseous sample, which was measured at and .
Give your answer to three significant figures.
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