MEDIUM
Diploma
IMPORTANT
Earn 100

Give the mechanism for the nitration of benzene. Use curly arrows to represent the movement of electron pairs.

Important Questions on Organic Chemistry [AHL]

MEDIUM
Diploma
IMPORTANT

Which statements about substitution reactions are correct?

I. The reaction between sodium hydroxide and 1-chloropentane predominantly follows an SN2 mechanism.

II. The reaction between sodium hydroxide and 2-chloro-2-methylbutane predominantly follows an SN2 mechanism.

III. The reaction of sodium hydroxide with 1-chloropentane occurs at a slower rate than with 1-bromopentane.

MEDIUM
Diploma
IMPORTANT
Which statement is correct about the enantiomers of a chiral compound?
MEDIUM
Diploma
IMPORTANT

Halogenoalkanes can undergo substitution reactions with potassium hydroxide solution.

State an equation for the reaction of C4H9Cl with KOH.

MEDIUM
Diploma
IMPORTANT

Substitution reactions may occur by either of two mechanisms namely SN1 or SN2. Outline the meaning of the term SN1.

HARD
Diploma
IMPORTANT

Predict the mechanism SN1 or SN2 expected for the reaction of the following halogenoalkanes with aqueous KOH.

  • 1-chlorobutane to form butan-1-ol
  • 2-chloro-2-methylpropane to form 2-methylpropan-2-ol.
MEDIUM
Diploma
IMPORTANT

Explain the mechanism of each of the following reactions using curly arrows to represent the movement of electron pairs.

  • 1-chlorobutane to form butan-1-ol
  • 2-chloro-2-methylpropane to form 2-methylpropan-2-ol.
HARD
Diploma
IMPORTANT

C5H11Br+NaOHC5H11OH+NaBr

The reaction with 2-bromo-2-methylbutane proceeds by an SN1 mechanism. Describe this mechanism using structural formulas and curly arrows to represent the movement of electron pairs.