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Solutions for Chapter 12: Synthesis

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Solutions for Chapter 12: Synthesis

Solutions for Chapter 12
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Since 41 problems in chapter 12: Synthesis have been answered, more than 73098 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. Chapter 12: Synthesis includes 41 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Arene

    A term used to classify benzene and its derivatives.

  • bond angles

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

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • dynamic equilibrium

    A state of balance in which opposing processes occur at the same rate. (Section 11.5)

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • fission

    The splitting of a large nucleus into two smaller ones. (Section 21.6)

  • Fourier-transform NMR (FT-NMR)

    In nuclear magnetic resonance (NMR) spectroscopy, a technique in which the sample is irradiated with a short pulse that covers the entire range of relevant rf frequencies.

  • Frost circle

    A graphic method for determining the relative energies of p MOs for planar, fully conjugated, monocyclic compounds.

  • Ground-state electron confi guration

    The lowest-energy electron confi guration for an atom or molecule.

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • lanthanide (rare earth) element

    Element in which the 4f subshell is only partially occupied. (Sections 6.8 and 6.9)

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • Meisenheimer complex

    Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • Shell

    A region of space around a nucleus that can be occupied by electrons, corresponding to a principal quantum number

  • substituents

    In nomenclature, the groups connected to the parent chain.

  • Syndiotactic polymer

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

  • Triol

    A compound containing three hydroxyl groups.

  • wedge

    In bond-line structures, a group in front of the page.

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