Lesson 3.3.3.1
3.3.3.1 Nucleophilic substitution Quiz: AQA Chemistry, Unit 3
20 questions
In partnership with Revision Ninja
Lesson 3.3.3.1, Nucleophilic substitution: 20 multiple choice questions for the AQA Chemistry (7405), Unit 3: Organic chemistry, written with Revision Ninja.
Host it live on the board and students join with a game code on their own devices, or revise alone with Free Play. The answers are revealed in the game.
The 20 questions
-
Why are halogenoalkanes more reactive than alkanes towards nucleophiles?
- Presence of free radicals
- Non-polar structure
- Higher molecular mass
- Polar C-X bond
-
Which nucleophile is used to hydrolyse halogenoalkanes to alcohols?
- OH-
- H+
- NO2+
- Br2
-
Which nucleophile produces a nitrile from a halogenoalkane?
- H2O
- NO3-
- CN-
- Cl2
-
Which nucleophile reacts with a halogenoalkane to form an amine?
- O2
- NH3
- Ar
- CH4
-
Which 1-haloalkane reacts fastest during nucleophilic substitution with hydroxide ions?
- 1-bromobutane
- 1-iodobutane
- 1-fluorobutane
- 1-chlorobutane
-
What factor determines the increasing rate of halogenoalkane hydrolysis down Group 17?
- Increasing electronegativity
- Decreasing bond enthalpy
- Decreasing molecular mass
- Increasing bond polarity
-
What precipitate forms when 1-chlorobutane undergoes hydrolysis in the presence of silver nitrate?
- Brown precipitate
- White precipitate
- Yellow precipitate
- Cream precipitate
-
Which silver halide precipitate is yellow?
- AgBr
- AgCl
- AgI
- AgF
-
Which halogenoalkane gives a cream precipitate in the silver nitrate test?
- Bromoalkane
- Iodoalkane
- Chloroalkane
- Fluoroalkane
-
Which halogenoalkane is the least reactive in nucleophilic substitution?
- 1-bromobutane
- 1-iodobutane
- 1-fluorobutane
- 1-chlorobutane
-
Which of these nucleophiles has a lone pair and is negatively charged?
- OH-
- H+
- CH3+
- BF3
-
How many species are involved in the rate-determining step of an SN2 reaction?
- Three
- Zero
- One
- Two
-
What is the product of the nucleophilic substitution of 1-bromopropane with aqueous OH-?
- Propanal
- Propene
- Propane
- Propan-1-ol
-
What product is formed when bromoethane reacts with excess aqueous ammonia?
- Ethylamine
- Ethanol
- Ethene
- Ethanenitrile
-
Which factor makes bromoalkanes more reactive in substitution than chloroalkanes?
- Greater bond enthalpy
- Lower bond enthalpy
- Higher bond polarity
- Smaller atomic radius
-
Which halogenoalkane is the most polar carbon-halogen bond?
- C-I
- C-Br
- C-F
- C-H
-
Why is the carbon atom in a carbon-halogen bond electron-deficient?
- Carbon donates protons
- Halogen is electronegative
- Halogen donates electrons
- Carbon is electronegative
-
Which halogenoalkane is tertiary?
- 2-chloro-2-methylpropane
- 1-chloropropane
- 2-chloropropane
- Chloromethane
-
Why does 1-iodobutane undergo hydrolysis faster than 1-chlorobutane?
- Lower bond enthalpy
- Higher bond enthalpy
- Smaller atomic size
- Greater bond polarity
-
What observation indicates the relative rate of halogenoalkane hydrolysis with silver nitrate?
- Precipitate formation rate
- Colour change duration
- pH change speed
- Effervescence rate
Related quizzes
- Nomenclature Quiz · 3.3.1.1 · 20 questions
- Reaction mechanisms Quiz · 3.3.1.2 · 20 questions
- Isomerism Quiz · 3.3.1.3 · 20 questions
- Fractional distillation of crude oil Quiz · 3.3.2.1 · 20 questions
- Modification of alkanes by cracking Quiz · 3.3.2.2 · 20 questions
- Combustion of alkanes Quiz · 3.3.2.3 · 20 questions
- Chlorination of alkanes Quiz · 3.3.2.4 · 20 questions
- Halogenoalkanes: Elimination Quiz · 3.3.3.2 · 20 questions
- Bonding Quiz · 3.3.10.1 · 20 questions
- Electrophilic substitution Quiz · 3.3.10.2 · 20 questions