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Chapter 18- Planar Kinetics of a Rigid Body: Work and Energy

Chapter 18- Planar Kinetics of a Rigid Body: Work and Energy

Chapter 18- Planar Kinetics of a Rigid Body: Work and Energy. STATICS and DYNAMICS- 11 th Ed., R . C. Hibbeler and A. Gupta Course Instructor: Miss Saman Shahid. Objective:.

By sevita
(388 views)

V8 Systembiologie

V8 Systembiologie

V8 Systembiologie. Idee: Methoden der Systembiologie ermöglichen die integrierte, simultane Betrachtung möglichst vieler zellulären Prozesse wichtige Fragen: (1) wie soll man die Gesamtheit der metabolischen Reaktionen beschreiben?

By rance
(139 views)

Goals

Goals

Chapter 9: Elimination Reactions of Alkyl Halides: Competition between Substitutions and Eliminations. Goals. After this chapter, you should be able to: Predict products of E2 and E1 reactions Determine stereochemistry of E2/E1 Products Determine whether S N 2, S N 1, E1 or E2 will occur.

By jorn
(136 views)

A Review of “Organic Chemistry” in First Term

A Review of “Organic Chemistry” in First Term

A Review of “Organic Chemistry” in First Term. Part A Some Important Concepts and Structure. 1. Different kinds of Organic Compounds. Alkanes Cycloalkanes Alkyl halides Alcohols. Saturated Compd. Hybrization Geometric structure. C atoms. Alkenes Alkynes Diene Arenes.

By odelia
(107 views)

Organic Chemistry

Organic Chemistry

Organic Chemistry. William H. Brown & Christopher S. Foote. Nucleophilic Substitution and  -Elimination. Chapter 8. Chapter 8. Nucleophilic Substitution. Nucleophilic substitution: any reaction in which one nucleophile is substituted for another at a tetravalent carbon

By didier
(409 views)

Organic Chemistry year 1 2008-2009

Organic Chemistry year 1 2008-2009

Organic Chemistry year 1 2008-2009. Professor Martin Wills Email: m.wills@warwick.ac.uk Office: C504 CONTENT OF LECTURES. Substitution reactions at saturated carbon atoms: ‘S N 2 and S N 1’.

By leiko
(105 views)

Unit 9, Chapter 28

Unit 9, Chapter 28

Unit 9, Chapter 28. CPO Science Foundations of Physics. Unit 9: The Atom. Chapter 28 Inside the Atom. 28.1 The Nucleus and Structure of the Atom 28.2 Electrons and Quantum States 28.3 The Quantum Theory. Chapter 28 Objectives. Describe the structure of an atom.

By elia
(159 views)

S N 1 Reactions

S N 1 Reactions

S N 1 Reactions. t-Butyl bromide undergoes solvolysis when boiled in methanol: Solvolysis: “cleavage by solvent” nucleophilic substitution reaction in which the solvent serves as the nucleophile. S N 1 Reactions.

By harva
(301 views)

COMPETITIVE NUCLEOPHILES

COMPETITIVE NUCLEOPHILES

COMPETITIVE NUCLEOPHILES. S N 1 REACTIONS. IN S N 1 REACTIONS ALL NUCLEOPHILES REACT EQUALLY WELL. HOH, H+. -. solvolysis. :Br:. +. slow. -. :Cl:. -. : I :. All react equally with the carbocation. The amounts of RCl, RBr and RI reflect their starting concentrations in

By ahmed-carson
(135 views)

A Review of “Organic Chemistry” in First Term

A Review of “Organic Chemistry” in First Term

A Review of “Organic Chemistry” in First Term. Part A Some Important Concepts and Structure. 1. Different kinds of Organic Compounds. Alkanes Cycloalkanes Alkyl halides Alcohols. Saturated Compd. Hybrization Geometric structure. C atoms. Alkenes Alkynes Diene Arenes.

By valentine-petty
(144 views)

COMPETITIVE NUCLEOPHILES

COMPETITIVE NUCLEOPHILES

COMPETITIVE NUCLEOPHILES. S N 1 REACTIONS. IN S N 1 REACTIONS ALL NUCLEOPHILES REACT EQUALLY WELL. HOH, H+. -. solvolysis. :Br:. +. slow. -. :Cl:. -. : I :. All react equally with the carbocation. The amounts of RCl, RBr and RI reflect their starting concentrations in

By destiny-davenport
(227 views)

Competition among S N 2, S N 1, E2,  and E1 Reactions

Competition among S N 2, S N 1, E2, and E1 Reactions

Competition among S N 2, S N 1, E2, and E1 Reactions. S N 2. S N 1. Competition among S N 2, S N 1, E2, and E1 Reactions. E2. E1. Rate-Determining Steps Revisited. S N 2. S N 1. E2. E1. Nucleophile Strength. The Free Energy Diagram. Hammond Postulate.

By saucier
(8 views)

S N 1 Reactions

S N 1 Reactions

S N 1 Reactions. S N 1: substitution, nucleophilic, unimolecular rate = k[substrate] Solvolysis is an S N 1 reaction in which the solvent is nucleophile. (CH 3 ) 3 CBr +CH 3 OH  (CH 3 ) 3 COCH 3 +HBr. boil. t -butyl bromide. Nuc. methyl t -butyl ether. S N 1 Reaction Mechanism.

By chebert
(1 views)


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