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Solutions for Chapter 18: Reactions at the a-Carbon of Carbonyl Compounds

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 18: Reactions at the a-Carbon of Carbonyl Compounds

Solutions for Chapter 18
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

Chapter 18: Reactions at the a-Carbon of Carbonyl Compounds includes 41 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Since 41 problems in chapter 18: Reactions at the a-Carbon of Carbonyl Compounds have been answered, more than 38878 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Aldehyde

    A compound containing a !CHO group

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • angle strain

    The increase in energy associated with a bond angle that has deviated from the preferred angle of 109.5°.

  • basic anhydride (basic oxide)

    An oxide that forms a base when added to water; soluble metal oxides are basic anhydrides. (Section 22.5)

  • bonding pair

    In a Lewis structure a pair of electrons that is shared by two atoms. (Section 9.2)

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • carbides.

    Ionic compounds containing the C2 22 or C42 ion. (22.3)

  • concentration

    The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • l amino acid

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

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • methylene group

    A CH2 group.

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • peptide

    A chain comprised of a small number of amino acid residues.

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • polyurethanes

    Polymers made up of repeating urethane groups, also sometimes called carbamate groups (!N!CO2!).

  • quaternary structure

    The structure that arises when a protein consists of two or more folded polypeptide chains that aggregate to form one protein complex.

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

  • SN2

    A bimolecular nucleophilic substitution reaction.

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