---
title: "Alkenes and Alkynes: Electrophilic Additions"
book: "University Chemistry — Year 1"
subject: chemistry
language: en
chapter: 25
exercises: 12
source: https://one-course.com/books/chemistry/2/en/chapter/25-alkenes-and-alkynes-electrophilic-additions
license: CC-BY-NC-SA-4.0
credit: "One Chemistry Book, One Course (one-course.com)"
---

# Chapter 25 — Alkenes and Alkynes: Electrophilic Additions

Shake an alkene with orange bromine water and the colour vanishes in seconds: the oldest test for a carbon–carbon double bond. Behind it is a mechanism. The $\pi$ electrons of the double bond, held less tightly than the $\sigma$ electrons and exposed above and below the plane of the molecule, attack an electron-poor reagent; the cation formed then captures a [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile). The same two steps add hydrogen halides, water and halogens to alkenes, decide which carbon receives which part of the reagent, and fix the stereochemistry of the product. This chapter develops them, with the rule a nineteenth-century chemist drew from observation and the [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) that explains it.

**You already know.**

[Carbocations](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates), their stability and [curly arrows](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-curly-arrow) ([Chapter 18](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#ch-b1-electronic-effects)); the Hammond postulate ([Proposition 9.6](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#prop-b1-elementary-steps-hammond)); $Z$/$E$ descriptors, (*R*)/(*S*), [meso compounds](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) and [racemic mixtures](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) ([Chapter 16](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#ch-b1-stereochemistry-in-depth)). The school volume (grade 12) listed the additions of alkenes without their mechanisms.

## 25.1 The $\pi$ bond as a nucleophile

**Definition 25.1 (Electrophilic addition).**

An *electrophilic addition* to a multiple bond is an addition whose first step is the attack of the $\pi$ electrons on an [electrophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) E: a cation is formed, which then captures a [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) Nu, so that E and Nu end on the two carbons of the former double bond.

The $\pi$ bond is the weaker of the two bonds of C=C ([Chapter 3](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#ch-b1-lewis-resonance-vsepr)), and its electrons lie away from the nuclei, above and below the plane: alkenes are [nucleophiles](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile), and react with acids, halogens and other [electrophiles](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) that leave saturated alkanes untouched.

## 25.2 Adding hydrogen halides: Markovnikov’s rule

![Addition of hydrogen bromide to propene. The π pair takes the proton, onto the terminal carbon, giving the secondary carbocation; the bromide ion adds to it: 2-bromopropane.](https://one-course.com/images/onecourse/chapters/chemistry-2/b1-electrophilic-additions/fig-dc262b8db3c9.svg)

*Addition of hydrogen bromide to propene. The $\pi$ pair takes the proton, onto the terminal carbon, giving the secondary [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates); the bromide ion adds to it: 2-bromopropane.*

**Proposition 25.2 (Markovnikov’s rule).**

In the addition of HX to an unsymmetrical alkene, the hydrogen goes to the carbon of the double bond that already carries more hydrogens (*Markovnikov’s rule*). In modern form: the [electrophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) adds so as to give the more stable [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates).

**Proof.** The proton transfer is the [rate-determining step](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#def-b1-elementary-steps-rds), endothermic, ending on a [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates). By the Hammond postulate ([Proposition 9.6](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#prop-b1-elementary-steps-hammond)) its [transition state](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#def-b1-elementary-steps-energy-profile) resembles the [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates), so the route to the more stable [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) has the lower barrier and is much faster. Putting the proton on the carbon with more hydrogens leaves the charge on the carbon with more alkyl groups, the more stable cation ([Proposition 18.8](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#prop-b1-electronic-effects-carbocation-order)). ∎

![Schematic energy profiles of the two possible additions of HBr to propene. The more stable secondary carbocation lies lower, and by the Hammond postulate so does the transition state that leads to it: the Markovnikov product forms much faster.](https://one-course.com/images/onecourse/chapters/chemistry-2/b1-electrophilic-additions/fig-0683a4d0fab5.svg)

*Schematic [energy profiles](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#def-b1-elementary-steps-energy-profile) of the two possible additions of HBr to propene. The more stable secondary [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) lies lower, and by the Hammond postulate so does the [transition state](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#def-b1-elementary-steps-energy-profile) that leads to it: the Markovnikov product forms much faster.*

**Definition 25.3 (Carbocation rearrangement).**

A *carbocation rearrangement* is the migration, within a [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates), of a hydrogen atom or an alkyl group with its [bonding pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) to the neighbouring cationic carbon, giving a more stable [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) (a 1,2-shift).

**Example 25.4 (A methyl shift).**

3,3-Dimethylbut-1-ene and hydrogen chloride give a secondary [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) next to a quaternary carbon; a methyl group moves across with its pair, making a tertiary cation. The main product is 2-chloro-2,3-dimethylbutane, whose skeleton differs from that of the alkene; 3-chloro-2,2-dimethylbutane is minor.

![Rearrangement of the 3,3-dimethylbutan-2-yl cation: a methyl group shifts to the cationic carbon, turning a secondary cation into a tertiary one, captured by chloride.](https://one-course.com/images/onecourse/chapters/chemistry-2/b1-electrophilic-additions/fig-6805b2a95020.svg)

*Rearrangement of the 3,3-dimethylbutan-2-yl cation: a methyl group shifts to the cationic carbon, turning a secondary cation into a tertiary one, captured by chloride.*

## 25.3 Adding water

**Definition 25.5 (Hydration of an alkene).**

The *hydration* of an alkene is the addition of water, catalysed by a [strong acid](https://one-course.com/books/chemistry/2/en/chapter/10-acidbase-equilibria-and-the-predominant-reaction-method#def-b1-predominant-reaction-strong-acid), giving an alcohol: the reverse of the [dehydration](https://one-course.com/books/chemistry/2/en/chapter/22-alcohols-activating-the-oh-group#def-b1-alcohol-activation-dehydration) of [Chapter 22](https://one-course.com/books/chemistry/2/en/chapter/22-alcohols-activating-the-oh-group#ch-b1-alcohol-activation).

The mechanism is that of HX with water as the [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile): protonation (Markovnikov), capture of the [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) by water, loss of a proton from the oxonium ion. Propene gives propan-2-ol, 2-methylpropene gives 2-methylpropan-2-ol. [Hydration](#def-b1-electrophilic-additions-hydration) and [dehydration](https://one-course.com/books/chemistry/2/en/chapter/22-alcohols-activating-the-oh-group#def-b1-alcohol-activation-dehydration) are the same equilibrium, $\ce{C3H6 + H2O <=> C3H8O}$; dilute aqueous acid and low temperature favour the alcohol, concentrated acid, heat and removal of the alkene favour the alkene ([Chapter 7](https://one-course.com/books/chemistry/2/en/chapter/7-describing-a-chemical-system-extent-activities-q-and-k#ch-b1-extent-q-and-k)).

## 25.4 Adding halogens: halonium ions and anti addition

**Definition 25.6 (Halonium ion, anti and syn addition).**

In the addition of $\ce{Br2}$ or $\ce{Cl2}$, the $\pi$ pair attacks one halogen atom while a [lone pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) of that atom bonds to the second carbon: a three-membered cyclic *halonium ion* forms, the other halogen leaving as halide. An addition in which the two new groups end on opposite faces of the former double bond is an *anti addition*; on the same face, a *syn addition*.

**Proposition 25.7 (Halogen addition is anti).**

The addition of bromine to an alkene is an [anti addition](#def-b1-electrophilic-additions-halonium): (*E*)-but-2-ene gives meso-2,3-dibromobutane, and (*Z*)-but-2-ene gives the [racemic mixture](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) of (*2R,3R*)- and (*2S,3S*)-2,3-dibromobutane.

**Proof.** The bromonium ion bridges one face of the former double bond; the bromide can only attack a carbon from the other face, opening the ring like an SN2 with inversion at that carbon. The two bromines end on opposite faces. For (*E*)-but-2-ene, attack at either carbon gives the same product, in which the two stereocentres are mirror images of each other: (*2R,3S*), meso. For (*Z*)-but-2-ene, attack at one carbon gives (*2R,3R*), at the other (*2S,3S*), with equal probability: a [racemic mixture](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers). The proof by drawing is [Exercise 25.10](#exo-b1-electrophilic-additions-10). ∎

![The bromonium ion formed from (E)-but-2-ene, and its opening by bromide from the opposite face (anti addition). The product has two stereocentres of opposite descriptors and an internal mirror plane in a suitable conformation: the meso compound, (2R,3S).](https://one-course.com/images/onecourse/chapters/chemistry-2/b1-electrophilic-additions/fig-a2d47c3027af.svg)

*The bromonium ion formed from (*E*)-but-2-ene, and its opening by bromide from the opposite face ([anti addition](#def-b1-electrophilic-additions-halonium)). The product has two stereocentres of opposite descriptors and an internal mirror plane in a suitable [conformation](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers): the [meso compound](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers), (*2R,3S*).*

**In the lab — Bromine water.**

Bromine is a dense, volatile, very toxic and corrosive liquid. The test for unsaturation uses dilute bromine water (or a commercial solution of a bromine [complex](https://one-course.com/books/chemistry/2/en/chapter/12-complexation#def-b1-complexation-complex)) in a fume cupboard, a few drops at a time; the disappearance of the orange colour signals an addition. In water, the bromonium ion is also captured by water, and a bromohydrin forms beside the dibromide.

## 25.5 Alkynes: additions and acetylides

Alkynes add HX and $\ce{X2}$ twice, each step as for alkenes (Markovnikov for HX). Their [hydration](#def-b1-electrophilic-additions-hydration), catalysed by acid and a mercury(II) salt, gives not the expected unsaturated alcohol but a ketone: an enol rearranges at once to the carbonyl compound, a process studied in the Year 2 volume.

**Definition 25.8 (Terminal alkyne, acetylide).**

A *terminal alkyne* $\ce{R-C#C-H}$ has its triple bond at the end of the chain. A [strong base](https://one-course.com/books/chemistry/2/en/chapter/10-acidbase-equilibria-and-the-predominant-reaction-method#def-b1-predominant-reaction-strong-acid) (sodium amide) removes its hydrogen, giving the *acetylide ion* $\ce{R-C#C-}$, a good carbon [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile).

**Proposition 25.9 (Acidity of terminal alkynes).**

The C–H bond of a [terminal alkyne](#def-b1-electrophilic-additions-acetylide) is far more acidic than those of alkenes and alkanes, though still much less acidic than water: acetylides are formed with amide ions, not with hydroxide, and are destroyed by water.

**Proof.** In the [acetylide ion](#def-b1-electrophilic-additions-acetylide) the [lone pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) occupies an orbital with half *s* character (*sp* carbon), held closer to the nucleus than the orbitals of *sp*$^2$ or *sp*$^3$ [carbanions](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates): it is more stable, and its conjugate acid stronger. It remains a much stronger base than hydroxide, so water protonates it. ∎

An acetylide attacks a primary halogenoalkane by SN2 (a new C–C bond, $\ce{R-C#C-}$ + $\mathrm{R'Br}$) or adds to a carbonyl like a [Grignard reagent](https://one-course.com/books/chemistry/2/en/chapter/21-organomagnesium-reagents#def-b1-organomagnesium-organometallic): another way to build carbon skeletons.

**Method 25.10 (Predicting an addition).**

1. Identify the [electrophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) ( $\ce{H+}$ , $\ce{Br2}$ ) and the [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) that will follow ( $\ce{X-}$ , water, the halide).
2. For $\ce{H+}$ : add it to the carbon that gives the more stable [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) (Markovnikov); check for a possible 1,2-shift.
3. For $\ce{X2}$ : bridge the [halonium ion](#def-b1-electrophilic-additions-halonium) and open it from the opposite face (anti); draw both possible attacks and compare the products (meso or racemic).
4. With water present, expect the alcohol (or the halohydrin) as well.

**History — Vladimir Markovnikov.**

![](https://one-course.com/images/onecourse/chapters/chemistry-2/b1-electrophilic-additions/img-3fe28766d5db.jpg)

Vladimir Markovnikov stated his rule in the nineteenth century, from the products he and others observed, long before [carbocations](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) or [curly arrows](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-curly-arrow) existed: a regularity of nature, written down before it could be explained. Its modern statement through [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) stability shows what a mechanism adds to an empirical rule: it says when the rule should fail. (Portrait from an obituary notice published in 1905, public domain, Wikimedia Commons.)

## 25.6 Exercises

**Exercise 25.1 ★.**

Give the main product of: propene + HCl; 2-methylpropene + HBr; 1-methylcyclohexene + HBr; but-2-yne + one equivalent of HCl.

**Solution of Exercise 25.1.**

2-Chloropropane; 2-bromo-2-methylpropane; 1-bromo-1-methylcyclohexane; 2-chlorobut-2-ene.

**Exercise 25.2 ★.**

Write the products of bromine with ethene, cyclohexene and propene. Name them.

**Solution of Exercise 25.2.**

1,2-Dibromoethane; *trans*-1,2-dibromocyclohexane; 1,2-dibromopropane.

**Exercise 25.3 ★.**

Which alcohol does the acid-catalysed [hydration](#def-b1-electrophilic-additions-hydration) of each alkene give: propene, 2-methylpropene, methylenecyclohexane?

**Solution of Exercise 25.3.**

Propan-2-ol; 2-methylpropan-2-ol; 1-methylcyclohexan-1-ol (Markovnikov in each case).

**Exercise 25.4 ★.**

Which of these compounds react with sodium amide: propyne, but-2-yne, propene, ethanol? Write the reactions.

**Solution of Exercise 25.4.**

Propyne ([terminal alkyne](#def-b1-electrophilic-additions-acetylide)): $\ce{CH3C#CH + NH2- -> CH3C#C- + NH3}$. Ethanol: $\ce{CH3CH2OH + NH2- -> CH3CH2O- + NH3}$. But-2-yne and propene have no acidic enough hydrogen.

**Exercise 25.5 ★★.**

Write the full mechanism of the [hydration](#def-b1-electrophilic-additions-hydration) of 2-methylpropene with [curly arrows](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-curly-arrow), and explain why the reverse reaction is favoured in hot concentrated acid.

**Solution of Exercise 25.5.**

The $\pi$ pair takes $\ce{H+}$ on the $\ce{CH2}$ carbon: tertiary cation $\ce{(CH3)3C+}$; a water [lone pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) bonds to it: $\ce{(CH3)3COH2+}$; a water molecule takes a proton: $\ce{(CH3)3COH}$. In hot concentrated acid water is scarce and the volatile alkene escapes: the reverse reaction, [dehydration](https://one-course.com/books/chemistry/2/en/chapter/22-alcohols-activating-the-oh-group#def-b1-alcohol-activation-dehydration), proceeds.

**Exercise 25.6 ★★.**

Explain with the Hammond postulate why 2-methylpropene reacts with HCl much faster than propene.

**Solution of Exercise 25.6.**

Protonation of 2-methylpropene gives a tertiary cation, of propene a secondary one. The rate-determining protonation has a [transition state](https://one-course.com/books/chemistry/2/en/chapter/9-reaction-mechanisms-elementary-steps-and-approximations#def-b1-elementary-steps-energy-profile) resembling the cation (Hammond): the more stable tertiary cation is reached over a lower barrier.

**Exercise 25.7 ★★.**

Bromine reacts with cyclohexene. Show that the product is *trans*-1,2-dibromocyclohexane, and say whether it is [chiral](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-stereocentre) and whether the product is optically active.

**Solution of Exercise 25.7.**

The bromonium ion bridges one face of the ring; bromide opens it from the other face: the two bromines end *trans*. The *trans* dibromide is [chiral](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-stereocentre) (no mirror plane), but bromide attacks the two carbons equally: the two [enantiomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) form in equal amounts, and the product is racemic, optically inactive.

**Exercise 25.8 ★★.**

Propose a mechanism for the addition of HCl to 3-methylbut-1-ene that gives mainly 2-chloro-2-methylbutane.

**Solution of Exercise 25.8.**

Protonation of C1 gives the secondary cation on C2, next to the tertiary C3 bearing a hydrogen; that hydrogen moves with its pair to C2 (a 1,2-hydride shift), leaving a tertiary cation on C3, captured by $\ce{Cl-}$: 2-chloro-2-methylbutane.

**Exercise 25.9 ★★.**

Propose a synthesis of hex-2-yne from propyne and a halogenoalkane, and of 1-phenylbut-2-yn-1-ol from propyne and benzaldehyde.

**Solution of Exercise 25.9.**

Propyne + sodium amide: the propynide ion; with 1-bromopropane (SN2): $\ce{CH3C#C-CH2CH2CH3}$, hex-2-yne. Propynide with benzaldehyde, then dilute acid: $\ce{C6H5CH(OH)C#CCH3}$, 1-phenylbut-2-yn-1-ol.

**Exercise 25.10 ★★★.**

Prove the stereochemistry of bromine addition to the two but-2-enes by drawing: bromonium ion, anti attack at each carbon, [Cram representation](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-representations) of the products, descriptors. Count the [stereoisomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers) formed in each case.

**Solution of Exercise 25.10.**

(*E*)-but-2-ene: bromonium on one face, bromide from the other at C2 or at C3; both attacks give the same compound, with descriptors (*2R,3S*): the [meso compound](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers), one stereoisomer. (*Z*)-but-2-ene: attack at C2 gives (*2S,3S*) (or its mirror image from the other face), attack at C3 (*2R,3R*); equal amounts: two [stereoisomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers), a [racemic mixture](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers).

**Exercise 25.11 ★★★.**

Bromine water with propene gives 1-bromopropan-2-ol as the main product. Explain the regiochemistry: why does water attack the more substituted carbon of the bromonium ion?

**Solution of Exercise 25.11.**

In the unsymmetrical bromonium ion, the more substituted carbon bears more of the positive charge (its C–Br bond is longer and weaker, like a nearly tertiary or secondary cation). Water, in large excess, attacks that carbon from the face opposite the bridge: 1-bromopropan-2-ol.

**Exercise 25.12 ★★★.**

A hydrocarbon $\ce{C5H10}$ decolourises bromine water and adds HBr to give 2-bromo-2-methylbutane; its [hydration](#def-b1-electrophilic-additions-hydration) gives 2-methylbutan-2-ol. Find two possible structures and propose a way to tell them apart.

**Solution of Exercise 25.12.**

$D = 1$: an alkene. 2-Methylbut-1-ene and 2-methylbut-2-ene both give the tertiary cation, hence 2-bromo-2-methylbutane and 2-methylbutan-2-ol. Their proton NMR spectra differ: two vinylic protons ($\ce{=CH2}$, singlets) for the first, one ($\ce{=CH-}$, a quartet) for the second.

## 25.7 Problem: Two Butenes and Bromine

**Problem 25.1.**

Weekend problem — the two but-2-enes, the bromonium mechanism, meso and racemic dibromides, their optical rotation and the mass obtained

A laboratory has two bottles of but-2-ene, one pure (*Z*), one pure (*E*), and treats $5.60\,\mathrm{g}$ of each with bromine in dichloromethane. Molar masses ($\mathrm{g}/\mathrm{mol}$): $\ce{C4H8}$ 56.0, $\ce{Br2}$ 159.8, $\ce{C4H8Br2}$ 215.8.

**Part I — The two alkenes.**

1. Draw ( *Z* )- and ( *E* )-but-2-ene and justify the descriptors.
2. Are they [stereoisomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers) ? [Enantiomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) or [diastereomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) ?
3. Why do they not interconvert at room temperature?
4. Which is the more stable, and why?
5. Write the overall equation of the addition of bromine.
6. How many stereocentres has 2,3-dibromobutane? How many [stereoisomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers) at most, and how many in fact?

**Part II — The mechanism.**

7. Write the formation of the bromonium ion with [curly arrows](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-curly-arrow) .
8. Why is a bridged bromonium ion formed rather than an open [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) ?
9. Write the opening of the ion by bromide.
10. Why does bromide attack from the face opposite the bridge?
11. What kind of addition results?
12. Why is the solvent dichloromethane and not water?

**Part III — The products.**

13. From ( *E* )-but-2-ene: draw the product of attack at C2 and give the descriptors of C2 and C3.
14. Same for attack at C3. Compare.
15. Show that the product is meso.
16. From ( *Z* )-but-2-ene: draw the two products and their descriptors.
17. In what proportions are they formed? Name the mixture.
18. Is the reaction stereospecific? Justify.

**Part IV — Rotation and mass.**

19. What optical rotation does the product of the ( *Z* ) alkene show?
20. Compute the amount of each alkene.
21. Compute the mass of dibromide expected from each at $85\,\%$ [yield](https://one-course.com/books/chemistry/2/en/chapter/7-describing-a-chemical-system-extent-activities-q-and-k#def-b1-extent-q-and-k-fractional-extent) .
22. State the [specific rotation](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-optical-activity) of the dibromide obtained from ( *E* )-but-2-ene, and the mass of it obtained.

**Solution of Problem 25.1.**

**1.** On each carbon $\ce{CH3}$ outranks H: (*Z*) has the two methyls on the same side, (*E*) on opposite sides. **2.** [Stereoisomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers) that are not mirror images: [diastereomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers). **3.** Rotation about C=C would break the $\pi$ bond, which costs far more energy than collisions provide at room temperature. **4.** (*E*): its methyl groups do not crowd each other. **5.** $\ce{C4H8 + Br2 -> C4H8Br2}$. **6.** Two equivalent stereocentres: at most four, in fact three ((*2R,3R*), (*2S,3S*) and the meso (*2R,3S*)). **7.** The $\pi$ pair attacks one Br atom of $\ce{Br2}$, the Br–Br pair leaves as $\ce{Br-}$, and a [lone pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) of the attacked bromine bonds to the second carbon: a three-membered bromonium ion. **8.** In the bridged ion every atom has an octet; an open secondary [carbocation](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-intermediates) would have a carbon with six electrons. **9.** A [lone pair](https://one-course.com/books/chemistry/2/en/chapter/3-lewis-structures-resonance-and-vsepr#def-b1-lewis-resonance-vsepr-lewis) of $\ce{Br-}$ bonds to one ring carbon; the C–Br bond of the bridge breaks, its pair going to the bridging bromine. **10.** The bridge occupies one face; as in SN2, the [nucleophile](https://one-course.com/books/chemistry/2/en/chapter/18-electronic-effects-and-reactive-intermediates#def-b1-electronic-effects-nucleophile) enters opposite the bond that breaks. **11.** An [anti addition](#def-b1-electrophilic-additions-halonium). **12.** Water would compete with bromide for the bromonium ion and give a bromohydrin. **13.** (*2R,3S*) (or (*2S,3R*), the same compound). **14.** The same compound. **15.** In a [conformation](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-isomers) with the two bromines eclipsed, a mirror plane passes between C2 and C3; the descriptors are opposite. **16.** (*2R,3R*) and (*2S,3S*). **17.** Equal amounts: a [racemic mixture](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers). **18.** Yes: the two diastereomeric alkenes give different products (meso against racemic). **19.** None: the two [enantiomers](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers) cancel. **20.** $5.60/56.0 = 0.100\,\mathrm{mol}$ each. **21.** $0.100 \times 0.85 \times 215.8 = 18.3\,\mathrm{g}$ each. **22.** **$[\alpha] = 0^\circ$ ([meso compound](https://one-course.com/books/chemistry/2/en/chapter/16-stereochemistry-in-depth#def-b1-stereochemistry-in-depth-enantiomers)), $18.3\,\mathrm{g}$**.