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Solutions for Chapter 24.9: KilianiFischer synthesis

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 24.9: KilianiFischer synthesis

Solutions for Chapter 24.9
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Chapter 24.9: KilianiFischer synthesis includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 1 problems in chapter 24.9: KilianiFischer synthesis have been answered, more than 34221 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • alternating copolymers

    A copolymer that contains an alternating distribution of repeating units.

  • bond angles

    The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)

  • Brønsted–Lowry base

    A substance (molecule or ion) that acts as a proton acceptor. (Section 16.2)

  • Constitutional isomers

    Compounds with the same molecular formula but a different connectivity of their atoms

  • covalent bond

    A bond formed between two or more atoms by a sharing of electrons. (Section 8.1)

  • covalent bond.

    A bond in which two electrons are shared by two atoms. (9.4)

  • cycloalkane

    An alkane whose structure contains a ring.

  • homotopic

    Protons that are interchangeable by rotational symmetry.

  • ionic hydrides

    Compounds formed when hydrogen reacts with alkali metals and also the heavier alkaline earths (Ca, Sr, and Ba); these compounds contain the hydride ion, H-. (Section 22.2)

  • kinetics

    A term that refers to the rate of a reaction.

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • N terminus

    For a peptide chain,the end that contains the amino group.

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • photodissociation

    The breaking of a molecule into two or more neutral fragments as a result of absorption of light. (Section 18.2)

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • Radical cation

    A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.

  • reduction

    A process in which a substance gains one or more electrons. (Section 4.4)

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • Transesterifi cation

    Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.

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