Phenol Understand the reaction of phenol with bromine water

Slides:



Advertisements
Similar presentations
PHENOL Acidity of phenol Reaction with sodium
Advertisements

TY 2002 Organic Mechanism 4 Nitration of Benzene.
HL Option G Organic Chemistry
Electrophilic Substitution Reactions of Benzene Aim: To describe the electrophilic substitution of arenes with concentrated nitric acid in the presence.
Delocalisation of Benzene Halogenation of Benzene
Phenol Aim: To introduce phenol and its properties To describe the reactions of phenol (i) With aqueous alkalis and sodium to form salts. (i) With bromine.
Advanced Higher Chemistry Unit 3 Aromatics. Aromatics Aromatics are hydrocarbons containing the benzene ring (C 6 H 6 ). The systematic name for the family.
Complete spot the bonding worksheet Work in pairs/small groups Write answers on paper or whiteboards (not the sheet)
Arenes Textbook p4-5.
Phenol.
Aromatic Compounds Phenol Chemistry. Syllabus Says... Phenols (f) describe the reactions of phenol: (i) with aqueous alkalis and with sodium to form salts,
Week 6 © Pearson Education Ltd 2009 This document may have been altered from the original Describe the preparation of aliphatic amines by substitution.
AMINES. Naming How many chains are coming off the Nitrogen atom in the amine Count the number of carbons in each chain Name each chain as a branch Add.
Reactions of benzene Benzene is electron rich. Electrophiles are electron pair acceptors. So electrophiles might be expected to add to benzene, saturating.
Phenols. HW: Hw1 Q 5 (12 marks) L.O.:  Describe the reactions of phenols with aqueous alkalis and with sodium to form salts  Discuss the roles of phenol.
Why do some solids dissolve in water but others do not? Why are some substances gases at room temperature, but others are liquid or solid? The answers.
8-2: Polarity. Remember electronegativity… An atom’s ability to attract electrons in a chemical bond. Polar bond: electrons are shared unequally between.
ml.
Arenes: Benzene Arenes are aromatic hydrocarbons containing 1 or more benzene rings. A benzene ring is a ring of 6 carbon atoms, each of which is also.
 Why do some solids dissolve in water but others do not?  Why are some substances gases at room temperature, but others are liquid or solid?  Why does.
Properties of Ionic and Covalent Compounds
Alkanes IB Chemistry Topic 10.2.
Why do some solids dissolve in water but others do not? Why are some substances gases at room temperature, but others are liquid or solid? The answers.
Why do some solids dissolve in water but others do not? Why are some substances gases at room temperature, but others are liquid or solid? The answers.
Week 2 © Pearson Education Ltd 2009 This document may have been altered from the original Explain the relative resistance to bromination of benzene compared.
Phenol L.O. To explore the effect of an OH group on the reactivity of the benzene ring. To be able to describe and explain the key reactions of phenol.
Reactions of arenes. Benzene and bromine can react together in an electrophilic substitution reaction.
Bromine is a red-brown liquid. When it is shaken with an alkene like ethene, it loses its colour.
Presentation of Group – IX Jonnaire B. H.Taher Crisol T. Carriedo.
Determining Bond Type.
Intermolecular Forces
No Bellwork 10/13/15 Review your grade report. Questions after class.
Intermolecular Forces
Alkanes and Alkenes Topic 10.2 part 1.
Mechanisms L.O. To know the mechanisms involved in heterolytic, electrophilic substitution of a benzene ring. Homework: 1. Test Yourself Q11-15 inclusive.
Solution Chemistry Unit 10 Chapter 16.
Electrophilic Substitution Reactions of Benzene
Polar Bonds and Molecules
Intermolecular Forces
Intermolecular forces
Polarity within a Molecule
Reactions with alkenes
Intermolecular Forces
Naming: carbon chain stem + oic
Group 7 The Halogens.
Solutions College Chemistry.
Polar Bonds Chemistry Mr. Scott.
Chemistry of Life Properties of Water.
Ch 2 notes Honors Biology Book.
7.13 – NOTES Solubility of Molecules
Chemistry of Life Properties of Water.
Intermolecular attractions
Wonderful Water 1st activity – Gently bend 4-5 toothpicks. Place in a star formation. Add a few drops of water to the center of the star. With a partner,
Chapter 8 Covalent Bonding 8.4 Polar Bonds and Molecules
Intermolecular Forces
There are two major classes of organic chemicals aliphatic : straight or branched chain organic substances aromatic or arene: includes one or more ring.
Covalent Bonding.
Alkanes IB Chemistry Topic 10.2.
7.11 – NOTES Solubility of Molecules
Covalent Bonding.
A guide for A level students KNOCKHARDY PUBLISHING
Functional Groups and Their Properties
PHENOLS.
Bonding and Forces.
What is an element? Particle Relative charge Relative mass
Chapter 8 Covalent Bonding 8.4 Polar Bonds and Molecules
Presentation transcript:

Phenol Understand the reaction of phenol with bromine water Understand reasons for the relative ease of bromination of phenol compared with benzene

What reagents and conditions are required for the bromination of benzene? Catalyst (Halogen carrier) Heated Under reflux

Room Temperature Bromine Water What reagents and conditions are required for the bromination of phenol? Room Temperature Bromine Water

What is the obvious difference about the bromination of benzene and the bromination of phenol?

Discuss the following question…. Why do you think the reaction between phenol and bromine happens more readily than with benzene?

Reasons why… Oxygen in the OH group has lone pairs of electrons  these e- can merge with the electrons in the delocalised pi (P) bond Electron density above and below the ring of atoms is increased  referred to as ‘activation’ because the molecule is now much more reactive towards electrophiles Bromine molecules, although usually non-polar, are polarised as they approach the benzene ring. Eventually, the Br-Br bond breaks and the Br+ electrophile attacks the benzene ring.

What is this compound?

Phenolphthaelin

Phenolphthaelin Colourless Pink

Questions Suggest why phenol is a solid at room temperature and is slightly soluble in water Write an equation for the formation of TCP from phenol

Answers Due to permanent dipole-dipole attractions due to the electronegativity of the oxygen - but is mainly due to hydrogen bonding. Hydrogen bonds can form between a lone pair on an oxygen on one molecule and the hydrogen on the -OH group of one of its neighbours. Phenol is moderately soluble in water - about 8 g of phenol will dissolve in 100 g of water. If you try to dissolve more than this, you get two layers of liquid. The top layer is a solution of phenol in water, and the bottom one a solution of water in phenol. The solubility behaviour of phenol and water is complicated, and beyond UK A level. Phenol is somewhat soluble in water because of its ability to form hydrogen bonds with the water. C6H5OH + 3Cl2  C6H2Cl3OH + 3HCl

d