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Solutions for Chapter 14.7: Acidity of 1-Alkynes

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 14.7: Acidity of 1-Alkynes

This expansive textbook survival guide covers the following chapters and their solutions. Since 8 problems in chapter 14.7: Acidity of 1-Alkynes have been answered, more than 36677 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 14.7: Acidity of 1-Alkynes includes 8 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alditol

    The product obtained when the aldehyde group of an aldose is reduced.

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • Aldonic acid

    The product formed when the !CHO group of an aldose is oxidized to a !COOH group

  • alkane

    A hydrocarbon that lacks p bonds.

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • alkylthio group

    An SR group.

  • Androgen

    A steroid hormone, such as testosterone, that mediates the development of sexual characteristics of males.

  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • atomic radius

    An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)

  • calcination

    The heating of an ore to bring about its decomposition and the elimination of a volatile product. For example, a carbonate ore might be calcined to drive off CO2. (Section 23.2)

  • chelating agent

    A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)

  • covalent bond

    A bond that results when two atoms share a pair of electrons.

  • divalent

    An element that forms two bonds, such as oxygen.

  • excited state

    A state that is achieved when a compound absorbs energy.

  • molecule

    A chemical combination of two or more atoms. (Sections 1.1 and 2.6)

  • pH

    The negative log in base 10 of the aquated hydrogen ion concentration: pH = -log3H+4. (Section 16.4)

  • reaction mechanism

    A detailed picture, or model, of how the reaction occurs; that is, the order in which bonds are broken and formed and the changes in relative positions of the atoms as the reaction proceeds. (Section 14.6)

  • second law of thermodynamics

    A statement of our experience that there is a direction to the way events occur in nature. When a process occurs spontaneously in one direction, it is nonspontaneous in the reverse direction. It is possible to state the second law in many different forms, but they all relate back to the same idea about spontaneity. One of the most common statements found in chemical contexts is that in any spontaneous process the entropy of the universe increases. (Section 19.2)

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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