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    Bi Functional

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    Mirza Tatsuya
    This document outlines the key concepts and learning outcomes for a course on bifunctional chemistry. The course will cover keto-enol tautomerism, reactions of enols and enolates including C-Hal and C=N-OH bond formation, aldol reactions, Claisen and Dieckmann reactions, reactions with alkylating agents, conjugate additions, and comparisons of related reactions involving enamines, silyl enol ethers, nitroalkanes, and cyanoalkanes. Upon completing the course, students will be able to predict and draw products of these various reactions of enols and enolates, as well as discuss factors controlling tautomeric stability.

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    Bi Functional

    Uploaded by

    Mirza Tatsuya
    224 views40 pages
    This document outlines the key concepts and learning outcomes for a course on bifunctional chemistry. The course will cover keto-enol tautomerism, reactions of enols and enolates including C-Hal and C=N-OH bond formation, aldol reactions, Claisen and Dieckmann reactions, reactions with alkylating agents, conjugate additions, and comparisons of related reactions involving enamines, silyl enol ethers, nitroalkanes, and cyanoalkanes. Upon completing the course, students will be able to predict and draw products of these various reactions of enols and enolates, as well as discuss factors controlling tautomeric stability.

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    This document outlines the key concepts and learning outcomes for a course on bifunctional chemistry. The course will cover keto-enol tautomerism, reactions of enols and enolates including C-Hal and C=N-OH bond formation, aldol reactions, Claisen and Dieckmann reactions, reactions with alkylating agents, conjugate additions, and comparisons of related reactions involving enamines, silyl enol ethers, nitroalkanes, and cyanoalkanes. Upon completing the course, students will be able to predict and draw products of these various reactions of enols and enolates, as well as discuss factors controlling tautomeric stability.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    224 views40 pages

    Bi Functional

    Uploaded by

    Mirza Tatsuya
    This document outlines the key concepts and learning outcomes for a course on bifunctional chemistry. The course will cover keto-enol tautomerism, reactions of enols and enolates including C-Hal and C=N-OH bond formation, aldol reactions, Claisen and Dieckmann reactions, reactions with alkylating agents, conjugate additions, and comparisons of related reactions involving enamines, silyl enol ethers, nitroalkanes, and cyanoalkanes. Upon completing the course, students will be able to predict and draw products of these various reactions of enols and enolates, as well as discuss factors controlling tautomeric stability.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PDF, TXT or read online from Scribd
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    of 40

    BIFUNCTIONAL CHEMISTRY (06522)

    Contents Overview Keto-enol tautomerisation Reactions of enols: C-Hal and C-N=O bond formation Reactions of enols and enolates with aldehydes and ketones Reactions of enolates with acylating agents Reactions of enolates with alkylating agents Conjugate additions: the Michael reaction Reactions of enol and enolate-like molecules Learning outcomes: At the end of the course you will be able to: 1. Keto-enol tautomerisation Demonstrate the mechanisms of both acid and base-catalysis of tautomerisation and draw tautomeric form(s) of a given molecule. Discuss factors controlling tautomeric stability. 2. Enols and enolates: C-Hal and C=N-OH bond formation Work out the products arising from the reaction of enols or enolates with halogens and the + NO ion. 3. Enols and enolates: the aldol reaction Work out the product(s) arising from the reaction of enols or enolates with aldehydes or ketones. 4. Enolates: the Claisen and Dieckmann reactions Work out the product(s) arising from the reaction of enolates with esters, anhydrides and acid chlorides. 5. Reactions of enolates with alkylating agents Work out the product(s) arising from the reaction of enolates with alkyl halides. 6. -Keto esters and 1,3-diesters Demonstrate the use of -keto esters and 1,3-diesters as stable enolate equivalents for such reactions, with the subsequent decarboxylation process. 7. Reactions of enolates with ,-unsaturated carbonyl compounds Work out the product(s) arising from the conjugate addition reactions of stable enolates with ,-unsaturated carbonyl compounds. 8. Enamines and Silyl Enol Ethers Compare the reactions of simple enamines and enol ethers with those of enols and enolates. 9. Nitroalkanes and cyanoalkanes Compare the reactions of the anions of nitroalkane and cyanoalkanes with those of enolates. Suggested reading

    Organic Chemistry, J. Clayden, N. Greeves, S. Warren and P. Wothers, Oxford University

    Press. Mainly Chapters 21, 26, 27, 28, 10, 29. Background / revision: Chapters 6, 12, 14 (reactions of aldehydes, ketones and esters lectures from year 1) Also recommended is Chemisty Of The Carbonyl Group, A Programmed Approach To Organic Reaction Mechanisms, S. Warren (Wiley, 1974) Bifunctional Compounds, RS Ward, OP (Oxford Primer No. 17): useful in parts Similar chapters will be found in all Organic Chemistry texts, e.g. T. Solomons & C. Fryhle, F. Carey, Maitland Jones etc. See http://www.hull.ac.uk/php/chsanb/teaching.html for a full set of notes and past final paper questions with answers. Other problems are also available to supplement your work book (module 06524 / 06013) which you must complete the as the course progresses. Dr AN Boa, C301, [email protected]

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