Sturtural Formula, Condensed Formula and Isomerism
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Sturtural Formula, Condensed Formula and Isomerism — Free MYP4 Chemistry Practice Questions
1QuestionStructural/displayed formulaConcept Practice
3 marks~5 minCriterion A
The diagram below shows the structural formula of a hydrocarbon molecule.
a
Deduce the total number of carbon atoms and the total number of hydrogen atoms present in this molecule. [2]
b
Explain, using the bonds shown in the diagram, why this molecule is classified as saturated. [1]
Solutions
2QuestionInterpreting skeletal diagramsAssessment Practice
2 marks~3 minCriterion C
The skeletal diagram below shows 3-methylpentane.
a
Deduce the condensed structural formula of 3-methylpentane from the skeletal diagram. Show your working by identifying each carbon group in the main chain and at the branch point. [1]
b
A student claims that CH3CH2CH(CH3)CH2CH3 and CH3CH(CH3)CH2CH2CH3 represent different compounds. Evaluate this claim. [1]
Solutions
3QuestionStructural/displayed formulaAssessment Practice
8 marks~12 minCriterion D
A chemical company produces a plastic using 2-methylpentane, a branched-chain alkane. To improve biodegradability, they propose substituting it with n-hexane, its straight-chain isomer. However, n-hexane poses greater toxicity risk to aquatic organisms. Both compounds share the molecular formula C6H14.
a
Draw the structural formula for each compound, clearly showing all bonds. [2]
b
Explain why n-hexane is expected to biodegrade more readily than 2-methylpentane. [2]
c
Evaluate the environmental and societal trade-offs of this substitution, including the limitations of assuming that all straight-chain alkanes biodegrade at the same rate under real landfill conditions. [4]
Solutions
4QuestionStructural/displayed formulaAssessment Practice
6 marks~9 minCriterion B
The molecular formula C4H10O represents several structural isomers containing a hydroxyl group (−OH).
a
Construct the displayed formulas for all structural isomers of C4H10O, ensuring every bond and atom is clearly shown. [2]
b
Describe the pattern in how the carbon skeleton and the position of the −OH group vary across the isomers drawn in part (a). [2]
c
Using the pattern identified in part (b), deduce the number of structural isomers of C5H12O that contain an −OH group. Justify your answer by systematically accounting for each carbon skeleton and each possible −OH position. [2]