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Halogenalkanes

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What are the two types of reactions that can occur with haloalkanes?

Back (Answer)

Only elimination or substitution reactions can occur

#2
Front (Question)

Describe and explain nucleophilic substitution

Back (Answer)

The C atom of the haloalkane is slightly positive, as the halogen it is attached to is more electronegative (and weaker). This means the negative nucleophile is attracted to the C The nucleophile bonds to the C, causing the halogen bond to break (weakest bond, can only have 4 bonds)

#3
Front (Question)

State what is meant by the term nucleophile

Back (Answer)

An electron pair donater.

#4
Front (Question)

What is hydrolysis?

Back (Answer)

Splitting molecules using water

#5
Front (Question)

How can we test for halogenoalkanes? (brief)

Back (Answer)

Do a substitution reaction which turns the halogen into a halide ion Then test for that ion with silver nitrate soln.

#6
Front (Question)

Describe how you would test for haloalkanes

Back (Answer)

Warm the haloalkane with NaOH soln. in a mix of ethanol and H2O Halogen displaced to become an ion Acidify with dilute nitric acid and then add silver nitrate Various precipitates may be formed You can confirm the precipitate by adding ammonia soln.

#7
Front (Question)

Why do you acidify the halide ion mixture with nitric acid?

Back (Answer)

To prevent any unreacted OH- ions reacting with the silver and giving a confusing precipitate

#8
Front (Question)

Adding silver nitrate soln. to a halide ion produces a white precipitate. What ion is it?

Back (Answer)

Cl-

#9
Front (Question)

Adding silver nitrate soln. to a halide ion produces a very pale yellow precipitate. What ion is it?

Back (Answer)

I-

#10
Front (Question)

Adding silver nitrate soln. to a halide ion produces a very pale cream precipitate. What ion is it?

Back (Answer)

Br-

#11
Front (Question)

What are the conditions for haloalkane substitution by OH- ions?

Back (Answer)

Aqueous and warm

#12
Front (Question)

What are the conditions for haloalkane substitutions by CN- ions?

Back (Answer)

Aqueous/alcohol Warm

#13
Front (Question)

What is produced by haloalkane substitution with CN- ions?

Back (Answer)

A nitrile

#14
Front (Question)

What are the conditions for haloalkane substitution by NH3?

Back (Answer)

Excess ammonia (NH3) Sealed tube

#15
Front (Question)

Give a general reaction for the substitution of a haloalkane by NH3

Back (Answer)

R-X + 2NH3 –> R-NH2 = NH4+X-

#16
Front (Question)

In substitution by NH3, NH3 acts in two ways. What are they?

Back (Answer)

As a nucleophile and as a base

#17
Front (Question)

What are the reagents and conditions for elimination reactions?

Back (Answer)

Reagents - NaOH/KOH Conditions - dissolved in ethanol

#18
Front (Question)

Describe and explain elimination reaction

Back (Answer)

The OH- takes one of the Hs - its electrons go to the C it was previously attached to These two electrons move to form double bond b/wn the 2 C atoms The approach of those electrons repels the electrons in the C-Br bond right out onto the bromine The Br is thrown off as a negative ion

#19
Front (Question)

What does CFC stand for?

Back (Answer)

Chlorofluorocarbons

#20
Front (Question)

What are the common uses of CFCs and why?

Back (Answer)

Low toxicity, low reactivity and low flammability led to common use as refrigerants and aerosol propellants

#21
Front (Question)

What is the ozone layer?

Back (Answer)

A thin layer of the atmosphere consisting of O3, that filters out some UV

#22
Front (Question)

What does the ozone layer do?

Back (Answer)

Filter out shorter wavelengths of UV light that would be harmful to most life in larger doses

#23
Front (Question)

Why do HCFCs not affect the ozone layer?

Back (Answer)

They don’t have the C-Cl bond

#24
Front (Question)

What is an ozone molecule?

Back (Answer)

O3