'Nucleophilic substitution reactions' presentation slideshows

Chem 150 Unit 8 - Organic Molecules III Alcohols, Thiols, Ethers, Aldehydes and Ketones

Chem 150 Unit 8 - Organic Molecules III Alcohols, Thiols, Ethers, Aldehydes and Ketones.

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Nucleophilic Substitution Reactions (Substitution at sp 3 -hybridized Carbon)

Nucleophilic Substitution Reactions (Substitution at sp 3 -hybridized Carbon). Halides are electronegative elements. Thus, in the case of an alkyl halide, R-X the halide atom can leave from carbon, taking the shared pair of electrons with it.

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Basic Organc Chemistry III

Review of Carbon Atom.

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Organic Chemistry

Organic Chemistry. Chapter 8. Substitution and Elimination. If an sp 3 C is bonded to electronegative atom Substitution reactions and Elimination reactions are possible. This chapter is all about substitution. example. S N 2 and S N 1 Reactions.

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Halogenoalkane compounds and Nucleophilic Substitution

Halogenoalkane compounds and Nucleophilic Substitution. 30.1 Introduction 30.2 Nomenclature of Halogeno-compounds 30.3 Physical Properties of Halogeno-compounds 30.4 Preparation of Halogeno-compounds 30.5 Nucleophilic Subsititution Reaction 30.6 Elimination Reactions. 30.1.

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7. Alkyl Halides

7. Alkyl Halides. What Is an Alkyl Halide. These are compounds containing a halogen bonded to a carbon atom. . The Frog. What Is an Alkyl Halide. These are compounds containing a halogen bonded to a carbon atom. . Naming Alkyl Halides . Identify the longest continuous carbon chain

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HL organic chemistry topic 20

HL organic chemistry topic 20. More functional groups Amines NH 2 Draw 1-aminopropane (propanamine) and give condensed formula. Methylamine (old) aminomethane IUPAC 1,6-diaminohexane. 1-butylamine, 1-butanamine, 1-aminobutane (all the same). Secondary amines.

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Organic Chemistry year 1 2011-2012

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Chapter 7 Alkyl Halides

Chapter 7 Alkyl Halides. ??????. ?? , ???. 7.1 Naming Alkyl Halides. 7.2 Preparing Alkyl Halides. The most general method for preparing alkyl halides is to make them from alcohols,. The reaction works best with tertiary alcohols . Primary and secondary alcohols react much more slowly.

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ALCOHOL

ALCOHOL. By Puan Azduwin Khasri 6 th NOVEMBER 2012. INTRODUCTION. Reaction of Alcohol. SUBSTITUTION. ELIMINATION (DEHYDRATION). OXIDATION. Others. SULFONATE ESTER. ALKYL HALIDE. KETONE ALDEHIDE CARBOXILIC ACID. ALKENE. Nucleophilic substitution of Alcohol.

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Chapter 6: Organic Halogen Compounds; Substitution and Elimination Reactions

Chapter 6: Organic Halogen Compounds; Substitution and Elimination Reactions. Nucleophilic Substitution. Examples of nucleophilic substitution reactions Nucleophile Substrate Leaving group. Reaction of sodium ethoxide with bromoethane. Nucleophilic Substitution Mechanism. S N 2 Mechanism.

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Chapter 3 BIOMOLECULES

Chapter 3 BIOMOLECULES. Chapter 3: You will be tested on pp. 53-69. Hydroxyl (alcohol) Carbonyl (aldehyde) (ketone) Carboxyl Methyl Ethyl Phenyl. Amino Amido Guanidino Imidazole Sulfhydryl Disulfide Phosphoryl. Ester Thioester Ether Anhydride Mixed anhydride

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Preparation

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Chapter 3 Biomolecules pages 53-73

Chapter 3 Biomolecules pages 53-73. 99% of the mass of most cells is H, O, N, and C These are the smallest elements that can form 1,2,3 and 4 bonds. Required in grams/day Required in milligrams or less/day. Biomolecules are complex, but are made up of simpler components.

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CHM1C3 Introduction to Chemical Reactivity of Organic Compounds Prof Jon A Preece

CHM1C3 Introduction to Chemical Reactivity of Organic Compounds Prof Jon A Preece j.a.preece@bham.ac.uk www.nanochem.bham.ac.uk Teaching Resources Username: Undergradchem Password: Preece57nano. www.nanochem.bham.ac.uk. Teaching Resources. Username: Undergradchem.

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IONIC LIQUIDS

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Chapter 7 Elimination Reactions

Chapter 7 Elimination Reactions. Unimolecular Elimination, E1 Elimination Reactions Removal of L.G. and H, but no substitution Formation of a C==C double bond Solvolysis of 2-bromo-2-methylpropane actually gives 2 products Rate of reaction for both products = k[haloalkane] E1

550 views • 8 slides