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CHE1502 EXAM PACK 2023 - DISTINCTION GUARANTEED

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Well-structured CHE1502 EXAM PREPARATION PACK - DISTINCTION GUARANTEED. Contains recent exam questions and answers, and Summarised study notes. All you need to pass the OCTOBER NOVEMBER 2023 EXAMS

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  • October 4, 2023
  • 832
  • 2023/2024
  • Exam (elaborations)
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CHE1502
EXAM PACK
 Recent exam questions and answers
 Summarised study notes
 Exam tips and guidelines


DISCLAIMER & TERMS OF USE
1. Educational Aid: These study notes are designed to serve as educational aids and should not be considered as a
substitute for individual research, critical thinking, or professional guidance. Students are encouraged to
conduct their own extensive research and consult with their instructors or academic advisors for specific
assignment requirements.
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4. Limited Liability: The seller of these study notes shall not be held liable for any direct or indirect damages,
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provided.

,MAY 2017 CHE1502
SECTION B

Question 1 [20]


(a) Draw the resonance forms to show the delocalization of charges in the
following structure. Show the movement of electrons with curved arrows.




(4)




1 mark for each arrow
1 mark each for correct 2nd and 3rd structure




(b) Draw the Newman projection formulas of the MOST STABLE and LEAST
STABLE conformations of the following compound below. Label the
conformations accordingly.

, (6)




2 marks for each correct Newman projection and 1 mark for correct Least stable
and 1 mark for correct most stable label.
If Newman projections are wrong but most and/or least stable identification is
correct give 1 mark each.




(c) Draw the Lewis structure of any secondary alcohol and give the IUPAC of the
chosen compound.

(4)
Any secondary alcohol √

Lewis structure : all bonds and atoms must be shown and the electrons around
O √√

Correct IUPAC name √




(d) Formulate a detailed mechanism of the following nucleophilic substitution
reaction:

, Name the product according to the IUPAC nomenclature.
(6)




Firstly, carbocation formation:




√ √


Secondly, we redraw the carbocation (in 3-D format) and show the nucleophile
attacking from the bottom or top:




√ √ √ one of each step and the product


IUPAC name: 3-Methyl-3-methoxypentane √




Question 2 [20]


(a) Consider the following reaction:

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