M5L2 - MP Quiz - Rates Graphs and Orders

M5L2 - MP Quiz - Rates Graphs and Orders

12th Grade

15 Qs

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M5L2 - MP Quiz - Rates Graphs and Orders

M5L2 - MP Quiz - Rates Graphs and Orders

Assessment

Quiz

Chemistry

12th Grade

Hard

Created by

Chris Jennings

FREE Resource

15 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Define the term electrophile.

An electrophile is a species that accepts an electron pair to form a new covalent bond.

An electrophile is a species that donates an electron pair to form a new covalent bond.

An electrophile is a negatively charged ion that loses electrons easily.

An electrophile is a molecule that always acts as a base in chemical reactions.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

State reagents/conditions needed to turn an alkene to an alkane.

Hydrogen gas (H2) and a nickel catalyst (Ni) at 150°C.

Bromine water at room temperature.

Concentrated sulfuric acid and heat.

Aqueous potassium manganate(VII) at room temperature.

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

State the observations you would make when propene is bubbled through bromine water.

The orange color of bromine water decolorizes.

A white precipitate forms.

The solution turns blue.

Effervescence is observed.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Use structural formulae to write a balanced equation for the reaction that takes place when propene is bubbled through bromine water.

CH2=CH-CH3 + Br2 → CH2Br-CHBr-CH3 (using structural formulae for each compound).

CH3-CH2-CH3 + Br2 → CH2Br-CH2Br-CH3 (using structural formulae for each compound).

CH2=CH2 + Br2 → CH2Br-CH2Br (using structural formulae for each compound).

CH2=CH-CH3 + Br2 → CH2=CH-CH2Br + HBr (using structural formulae for each compound).

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Draw a mechanism for the reaction of propene with bromine water.

The mechanism is the electrophilic addition of Br2 to propene, showing the formation of a carbocation intermediate and the addition of Br- ion.

The mechanism is a free radical substitution, where Br2 forms radicals and substitutes a hydrogen atom on propene.

The mechanism is a nucleophilic substitution, where water attacks the double bond of propene directly.

The mechanism is an elimination reaction, where Br2 removes a hydrogen and a bromine atom from propene to form an alkyne.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Draw the two products from the reaction of HBr with propene.

1-bromopropane and 2-bromopropane.

1-chloropropane and 2-chloropropane.

1-bromopropane and 3-bromopropane.

2-bromopropane and 3-bromopropane.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Predict the Major and Minor Products when HBr reacts with propene.

Major product: 2-bromopropane; Minor product: 1-bromopropane.

Major product: 1-bromopropane; Minor product: 2-bromopropane.

Major product: 2-bromopropane; Minor product: 2-bromopropane.

Major product: 1-bromopropane; Minor product: 1-bromopropane.

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