Skip to ContentGo to accessibility pageKeyboard shortcuts menu
OpenStax Logo
Organic Chemistry

Summary of Reactions

Organic ChemistrySummary of Reactions

9 • Summary of Reactions

9 • Summary of Reactions

No stereochemistry is implied unless specifically indicated with wedged, solid, and dashed lines.

  1. Preparation of alkynes
    1. Dehydrohalogenation of vicinal dihalides (Section 9.2)
      The figure shows two reactions that give the same products named alkyne, water and KBr. The reactant in the first reaction is dihalide and in the second reaction is alkene.
    2. Alkylation of acetylide anions (Section 9.8)
      Acetylene reacts with sodium amide to produce sodium acetylide that further reacts with an alkyl bromide to give a terminal alkyne.
      A terminal alkyne reacts with sodium amide to produce sodium acetylide that further reacts with an alkyl bromide to give an internal alkyne.
  2. Reactions of alkynes
    1. Addition of HCl and HBr (Section 9.3)
      The figure shows an alkyne reacting with a hydrogen halide in ether to give a dihaloalkene. This further reacts with hydrogen halide in ether to form a tetrahaloalkane.
    2. Addition of Cl2 and Br2 (Section 9.3)
      The figure shows an alkyne reacting with a halide in dichloromethane to form an alkene. This further reacts with a halide and dichloromethane to form an alkane.
    3. Hydration (Section 9.4)

      (1) Mercuric sulfate catalyzed

      Alkyne reacts with sulfuric acid, water and mercuric sulfate to form an enol. This further forms a methyl ketone.

      (2) Hydroboration–oxidation

      Alkyne reacts with borane and hydrogen peroxide undergoing hydroboration–oxidation to form an aldehyde.
    4. Reduction (Section 9.5)

      (1) Catalytic hydrogenation

      The figure shows two catalytic hydrogenation reactions. The first reaction is an alkyne reacting to form an alkane. The second reaction is an alkyne reacting to form a cis alkene.

      (2) Lithium in liquid ammonia

      Alkyne reacts in the presence of lithium and ammonia to form a trans alkene.
    5. Conversion into acetylide anions (Section 9.7)
      Alkyne reacts with sodium amide and ammonia to form sodium acetylide ion and ammonia.
Order a print copy

As an Amazon Associate we earn from qualifying purchases.

Citation/Attribution

This book may not be used in the training of large language models or otherwise be ingested into large language models or generative AI offerings without OpenStax's permission.

Want to cite, share, or modify this book? This book uses the Creative Commons Attribution-NonCommercial-ShareAlike License and you must attribute OpenStax.

Attribution information
  • If you are redistributing all or part of this book in a print format, then you must include on every physical page the following attribution:
    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter
  • If you are redistributing all or part of this book in a digital format, then you must include on every digital page view the following attribution:
    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter
Citation information

© Jan 9, 2024 OpenStax. Textbook content produced by OpenStax is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike License . The OpenStax name, OpenStax logo, OpenStax book covers, OpenStax CNX name, and OpenStax CNX logo are not subject to the Creative Commons license and may not be reproduced without the prior and express written consent of Rice University.