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Topic : Phenol & Aniline
Presented by: Mohabbat Mandal Presented to:
ID:171-150-0-155 Laudmila Haque
Mehedi Hasan Naim Sr. Lecturer of Environmental Science
ID:171-151-0-155 BGMEA University of Fashion & Technology
Afrana Anam Any
ID:171-152-0-155
Shahadat Hossain
ID:171-153-0-155
Kamrul Islam Omi
ID:171-154-0-155
Content
1. Introduction
2. Phenol Preparations
3. Reactions with Phenol
4. Resonance of Phenol
5. Aniline Preparation
6. Reactions of Aniline
7. Resonance of Aniline
Phenol
• In organic chemistry, a class of chemical
compounds consisting of a hydroxyl group
(—OH) bonded directly to an aromatic
hydrocarbon group. The simplest of the
class is phenol, which is also called
carbolic acid 𝐶6 𝐻5OH.
Aniline
• Aniline is an organic compound consisting
of a phenyl group(C6H5) attached to an
amino group (—NH2) .The formula is
C6H5NH2.
Phenol Preparations
benzene sulfonic acid
chlorobenzene
cumene
diazonium salts
Acidic Oxidation
From Sodium Hydroxide
or by Base
From Sodium Hydroxide/
Chlorobenzene/Daw
process
By Hydrolysis
650k, 300atm
Reactions with Phenol
(Aryl ketone via C-acylation, a Friedel-Crafts reaction)
(ester via O-acylation, an esterification)
Acylation of Phenols
Halogenation
Carboxylation of Phenol
Aspirin
Acyl chloride
Resonance of Phenol
Phenol is acidic in nature. It will lose Hydrogen cation to form Phenoxide ion which is more
stable than Phenol. Resonance structures of Phenol:
Aniline Preparation
From Nitrobenzene
From chlorobenzene
From Benzoic acid
Reactions of Aniline
1.
2.
3.
4.
Resonance of Aniline
Basicity: Aniline is a weak base. ... Traditionally, the weak basicity of aniline is attributed to a
combination of inductive effect from the more electronegative sp2 carbon and resonance effects,
as the lone pair on the nitrogen is partially delocalized into the pi system of the benzene ring.
Thank you

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Phenol & Aniline

  • 1. Topic : Phenol & Aniline Presented by: Mohabbat Mandal Presented to: ID:171-150-0-155 Laudmila Haque Mehedi Hasan Naim Sr. Lecturer of Environmental Science ID:171-151-0-155 BGMEA University of Fashion & Technology Afrana Anam Any ID:171-152-0-155 Shahadat Hossain ID:171-153-0-155 Kamrul Islam Omi ID:171-154-0-155
  • 2. Content 1. Introduction 2. Phenol Preparations 3. Reactions with Phenol 4. Resonance of Phenol 5. Aniline Preparation 6. Reactions of Aniline 7. Resonance of Aniline
  • 3. Phenol • In organic chemistry, a class of chemical compounds consisting of a hydroxyl group (—OH) bonded directly to an aromatic hydrocarbon group. The simplest of the class is phenol, which is also called carbolic acid 𝐶6 𝐻5OH. Aniline • Aniline is an organic compound consisting of a phenyl group(C6H5) attached to an amino group (—NH2) .The formula is C6H5NH2.
  • 4. Phenol Preparations benzene sulfonic acid chlorobenzene cumene diazonium salts Acidic Oxidation From Sodium Hydroxide or by Base From Sodium Hydroxide/ Chlorobenzene/Daw process By Hydrolysis 650k, 300atm
  • 5. Reactions with Phenol (Aryl ketone via C-acylation, a Friedel-Crafts reaction) (ester via O-acylation, an esterification) Acylation of Phenols Halogenation Carboxylation of Phenol Aspirin Acyl chloride
  • 6. Resonance of Phenol Phenol is acidic in nature. It will lose Hydrogen cation to form Phenoxide ion which is more stable than Phenol. Resonance structures of Phenol:
  • 7. Aniline Preparation From Nitrobenzene From chlorobenzene From Benzoic acid
  • 9. 4.
  • 10. Resonance of Aniline Basicity: Aniline is a weak base. ... Traditionally, the weak basicity of aniline is attributed to a combination of inductive effect from the more electronegative sp2 carbon and resonance effects, as the lone pair on the nitrogen is partially delocalized into the pi system of the benzene ring.