11: Reactions of Alkyl Halides- Nucleophilic Substitutions and Eliminations

Athabasca University Chemistry 350 Organic Chemistry I · LibreTexts

0%

Contents

    Text

    Size
    100%
    Theme
    Typeface
    Line length
    Spacing

    From LibreTexts, under CC BY-NC-SA 4.0, as the source states it; its equations are written in TeX, which the PDF shows typeset. This page at LibreTexts.

    11: Reactions of Alkyl Halides- Nucleophilic Substitutions and Eliminations
    Learning Objectives

    After you have completed Chapter 11, you should be able to

    1. fulfill all of the detailed objectives listed under each individual section.
    2. use the reactions studied in this chapter with those from earlier ones when designing multistep syntheses.
    3. use the reactions and concepts discussed in this chapter to solve road map problems.
    4. define, and use in context, the key terms introduced.

    In this course, you have already seen several examples of nucleophilic substitution reactions; now you will see that these reactions can occur by two different mechanisms. You will study the factors that determine which mechanism will be in operation in a given situation, and examine possible ways for increasing or decreasing the rates at which such reactions occur. The stereochemical consequences of both mechanisms will also be discussed.

    Elimination reactions often accompany nucleophilic substitution; so these reactions are also examined in this chapter. Again you will see that two different mechanisms are possible, and, as in the case of nucleophilic substitution reactions, chemists have learned a great deal about the factors that determine which mechanism will be observed when a given alkyl halide undergoes such a reaction.


    11: Reactions of Alkyl Halides- Nucleophilic Substitutions and Eliminations is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.