Lesson 6C.2
6C.2 Electrophilic addition mechanisms and tests Quiz: Pearson Edexcel Chemistry, Unit 6
20 questions
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Lesson 6C.2, Electrophilic addition mechanisms and tests: 20 multiple choice questions for the Pearson Edexcel Chemistry (9CH0), Unit 6: Organic Chemistry I, written with Revision Ninja.
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The 20 questions
-
Which term best describes the role of an electrophile?
- Electron pair donor
- Free radical generator
- Proton acceptor
- Electron pair acceptor
-
What type of bond fission occurs when ethene reacts with bromine?
- Homolytic fission
- Thermal fission
- Heterolytic fission
- Photolytic fission
-
Where does a curly arrow start in an organic reaction mechanism?
- Reaction product
- Electron pair
- Atomic nucleus
- Positively charged atom
-
What is the intermediate formed in the electrophilic addition of Br2 to ethene?
- A carbocation, CH2BrCH2+
- A carbanion, CH2BrCH2-
- An ester, CH2BrCOOCH3
- A free radical, CH2BrCH2*
-
What colour change occurs when bromine water reacts with an alkene?
- Orange to colourless
- Blue to red
- Colourless to orange
- Purple to colourless
-
Why do alkanes not decolourise bromine water in the dark?
- No sigma bonds
- High polarity
- No pi bond
- Too reactive
-
Propene reacts with hydrogen bromide. What is the major product?
- 2-bromopropane
- Bromoethane
- 1,2-dibromopropane
- 1-bromopropane
-
Which type of carbocation is the most stable?
- Tertiary
- Methyl
- Secondary
- Primary
-
Why are secondary carbocations more stable than primary carbocations?
- Electronegativity
- Inductive effect
- Hydrogen bonding
- Steric hindrance
-
What is the major product when 2-methylpropene reacts with hydrogen chloride?
- 2-chloro-2-methylpropane
- 2-chloropropane
- 1,2-dichloro-2-methylpropane
- 1-chloro-2-methylpropane
-
Which atom acts as the electrophile in HBr addition to ethene?
- Carbon atom
- Bromine atom
- Bromide ion
- Hydrogen atom
-
What intermediate is formed in the first step of electrophilic addition of HCl to ethene?
- Carbocation
- Transition state
- Free radical
- Carbanion
-
Which compound forms as the major product when but-2-ene reacts with HBr?
- 2-methylpropyl bromide
- 2-bromobutane
- 1-bromobutane
- 1,2-dibromobutane
-
Which intermediate is formed when propene reacts with H+ in the first step of hydration?
- A secondary carbocation, CH3CH+CH3
- A carbanion, CH3CH-CH3
- A primary carbocation, CH3CH2CH2+
- A radical, CH3CH*CH3
-
What is the expected colour change of acidified potassium manganate(VII) when reacted with an alkene?
- Blue to pink
- Colourless to green
- Yellow to orange
- Purple to colourless
-
What is the correct name for the product of Br2 with but-1-ene?
- 1,1-dibromobutane
- 2,3-dibromobutane
- 1,4-dibromobutane
- 1,2-dibromobutane
-
Why is the reaction of ethene with bromine classified as addition rather than substitution?
- Hydrogen atoms substituted
- No atoms eliminated
- Carbon chain shortened
- Double bond formed
-
What factor determines the regioselectivity of electrophilic addition to an unsymmetrical alkene?
- Electronegativity difference
- Electrophile size
- Carbocation stability
- Bond enthalpy
-
What effect from attached alkyl groups stabilises a tertiary carbocation?
- Inductive effect
- Resonance effect
- Steric effect
- Hydrogen bonding
-
What is the major product when propene reacts with aqueous bromine?
- 1-bromopropan-2-ol
- 2-bromopropan-1-ol
- 1,2-dibromopropane
- 2-bromopropane
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