Solutions for Chapter 15.2: Preparation of Alcohols by Reduction of Aldehydes and Ketones

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 15.2: Preparation of Alcohols by Reduction of Aldehydes and Ketones

Solutions for Chapter 15.2
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Chapter 15.2: Preparation of Alcohols by Reduction of Aldehydes and Ketones includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 15.2: Preparation of Alcohols by Reduction of Aldehydes and Ketones have been answered, more than 10912 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • absorbance

    In UV-Vis spectroscopy, the value log (I0/I) where I0 is the intensity of the reference beam and I is the intensity of the sample beam.

  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • Alkyl group

    A group derived by removing a hydrogen from an alkane; given the symbol R!

  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • chiral

    An object that is not superimposable on its mirror image.

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • continuous spectrum

    A spectrum that contains radiation distributed over all wavelengths. (Section 6.3)

  • Contributing structures

    Representations of a molecule or ion that differ only in the distribution of valence electrons.

  • desulfurization

    The conversion of a thioacetal into an alkane in the presence of Raney nickel.

  • electrochemistry

    The branch of chemistry that deals with the relationships between electricity and chemical reactions. (Chapter 20: Introduction)

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • haloalkane

    An organic compound containing at least one halogen.

  • halogens

    Members of group 7A in the periodic table. (Section 7.8)

  • heterocycle

    A cyclic compound containing at least one heteroatom (such as S, N, or O) in the ring.

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • molecular equation

    A chemical equation in which the formula for each substance is written without regard for whether it is an electrolyte or a nonelectrolyte. (Section 4.2)

  • nucleophilic aromatic substitution

    A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.

  • Ribosomal RNA (rRNA)

    A ribonucleic acid found in ribosomes, the sites of protein synthesi

  • Twist-boat conformation

    A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.

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