Organic Chemistry Question Review (2026-08-12)

Question: What is the Chinese trivial name for the organic compound below?

A. 庚烷
B. 辛烷
C. 壬烷
D. 癸烷

Solution: D

4-propylheptane = isodecane

The molecular formula is still C_{10}H_{22} .

Question: Study the compound below:

(a) Notice the functional group(s). What will you call it as?
(b) What are the products when it is reacted with hot KMnO_4 / H^+ (aq)?

Solution:

(a) Alkyne (similar to cyanide)
(b) Carboxylic acid(aq) + CO_2 (g)

Question: Study the flow chart below:

(a) What reagent is missing for the last step?
(b) What solvent should be used to contain O_3 (g)?

Solution:

(a) H^+ / H_2O_2 (aq)
(b) CCl_4 (l)

Question: Alkyne can be converted to ketone by hydration.

(a) What reagents are commonly used?
(b) Name 2 alternative reagents.

Solution

(a) H_2O / H_2SO_4 (aq)
(b) HgSO_4 / H_2SO_4 (aq) or BH_3/ NaOH, H_2O_2 (aq)

Question: Study the flow chart below:

(a) What is the phase of the intermediate compound?
(b) What if Cu^+ or Ag^+ is used instead of Na?

Solution:

(a) Na (s) / NH_3 (l)
(b) Reddish-brown precipitate (for Cu^+) or Yellowish-white precipitate (for Ag^+) will be formed instead of colourless liquid

Question: Study the reaction below:

What is the actual reagent instead of X_2/H_2O (aq)?

Solution:

HOX (e.g. Hydrobromous acid HOBr) (aq)

X = Br or Cl

Question: Study the reaction below:

(a) What is the mole ratio of alkyne:HOX?
(b) What is the by-product of the reaction?

Solution:

(a) 1:2
(b) water molecules

Question: Study the compound below:

(a) What is it called?
(b) How can it be prepared?
(c) What will happen if we dilute it?

Solution:

(a) Sulphonic acid
(b) Adding cold concentrated Sulphuric acid on an alkene
(c) Increment of protons will convert it to alkane.

Question: Study the flow chart below:

Explain why the reaction is exothermic.

Solution:

  1. Ozonolysis is redox reaction (i.e. involving electron transfer)
  2. Bond formation > Bond breakdown

Last question:

Account for the difference of HX reactions with alkene as shown below:

Solution:

Note the difference of the reaction mechanisms.

The stability of carbocation is due to steric hindrance.