SuperExamSuperExam
Search papers…
Menu
DashboardBrowse papersRevision notesBooksSavedRevision packsMy progressAchievementsAI TutorMessages

Unlock worked solutions

Step-by-step answers by examiners. From €5/mo.

Try Premium free →
← Chemistry notes
Edexcel IAL·Chemistry·IAL Chemistry

Alkenes

15 min read

Bonding in alkenes, electrophilic addition reactions and their mechanism, Markovnikov's rule, and addition polymers.

Alkenes (CnH2nC_nH_{2n}Cn​H2n​) are unsaturated hydrocarbons with a reactive C=C double bond (a σ and a π bond). The π bond is a region of high electron density, so alkenes undergo electrophilic addition.

Electrophilic addition

The π electrons attack an electrophile (electron-poor species). General mechanism (e.g. HBr + ethene):

  1. The C=C π electrons attack the δ+ end of HBr, forming a carbocation and a bromide ion.
  2. The bromide ion attacks the carbocation, forming the product.

Use curly arrows (movement of an electron pair) in the mechanism.

Viewing only

This content is free to read on superexams.com and cannot be printed or downloaded.

Read the full note — free

Create a free account to read this note in full. Every free account gets 2 complete revision notes — no card needed.

Sign up free →Log in

More Chemistry notes

Atomic Structure & the Periodic Table

Amount of Substance (Moles)

Bonding & Structure

Shapes of Molecules, Polarity & Intermolecular Forces