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Summary AQA AS-level/A-level Halogenoalkanes full revision notes

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Notes on Halogenoalkane for AQA AS/A-level Chemistry | instant download | Struggling to memorise Halogenoalkane? These beautifully handwritten A-Level AQA Chemistry notes make the trickiest topics easier to understand and revise. Ideal for visual learners, these notes are neat, structured, and directly aligned with the AQA specification. Summarised information meaning concise knowledge. - Handwritten for clarity and visual learning - Covers the full ‘Halogenoalkane’ topic concisely - Perfect for quick revision or in-depth study - Digital PDF download – print or view on any device and instant access - uses exam question answers to learn key knowledge for subtopics Whether you're reviewing for mocks or prepping for your A-Level exams, these notes save you time and help lock in with easy-to-read visuals, definitions, and exam-style answer notes. Knowledge for many of the subtopics are in the form of answers to key exam questions so ticks important points when used to answer questions. No refunds as this is an electronic product but can contact if there are any issues with the product. Product should not be re-distributed or re-sold. Apologies for any tiny spelling mistakes as these have been handwritten on a device Trusted by students aiming for top grades– a must-have study tool for any serious A-Level student. Designed by an A-Level student (who got into Imperial for Medicine), for A-Level students – perfect for Year 12 & 13 revision! Good luck!

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alo alkanes
alkanes with 1 or more halogens attached to it
naminghalogeno alkanes
1 find longest carbon chain forms last partof name
2 names and positionsof halogenon molecules comes first prefix
prefixes fluoro chloro bromo iodo
use numbers to state their positions on carbon chain
must be in alphabetical order if more than 1 typeofhalogen
3 more than one of the same typeof halogen prefix with di tri tetra
e's
H
É Ice 1 bromo 1,1 dichloro 2 iodo ethane
boiling point trends ofhalogenoalkanes
b p increases down group
strengthof intermolecular forcesgovern the b p strongerthe
ee higherthe b p intermolecular
As youdescendgroup 7 no of e increases
more e means stronger van der waals forces betweenmoleculesand so
more energyneeded to overcome these forces b p increases down the group
Bond polarityandnucleophiles
halogens are more electronegative than carbon so pull e towards themserve
a covalent bond leads to a polar bond
e 91
HE É
polar bond means that theycan be attacked by nucleophiles
nucleophile a substance that is an e pair donor
eg CN NH3 OH
reaction with hydroxide ions overall equation R X NaOH ROH Nay
via nucleophilic substitution i R
alkylgroup X halogen
conditions
I Grano9989888SEE hydroxide sourceof ions
on
hot formed
ii
gtfo É n
I
n

reaction with cyanide ions
5
overall equation R X KIN Rent KX
via nucleophilic substitution 1 R alkylgroup X halogen
conditions
1 warm ethanolic potassiumcyanide source of CN ions
carried out under REFLUX
nitrileformed
Ekg n

reaction withammonia
n
g
c

overallequation H3CH2CH2NH3 CHzCHzNHz Nagel
via nucleophilic substitution
conditions
1 Heat with ethanolicammonia
2 Must have excess ammonia r amine formed

Ets
Eas ftp.t.IE
nucleophile 5baseiiitiI
t



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