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Solutions for Chapter 5.12: The E1 and E2 Mechanisms of Alcohol Dehydration

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 5.12: The E1 and E2 Mechanisms of Alcohol Dehydration

Solutions for Chapter 5.12
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This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 5.12: The E1 and E2 Mechanisms of Alcohol Dehydration have been answered, more than 35968 students have viewed full step-by-step solutions from this chapter. Chapter 5.12: The E1 and E2 Mechanisms of Alcohol Dehydration includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • [4+2]-cycloaddition

    A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.

  • Aldose

    A monosaccharide containing an aldehyde group

  • Allylic carbocation

    A carbocation in which an allylic carbon bears the positive charge.

  • angstrom

    A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)

  • Atactic polymer

    A polymer with completely random confi gurations at the chiral centers along its chain, as, for example, atactic polypropylene

  • Coupling constant

    The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • f-block metals

    Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)

  • fingerprint region

    The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • oxyanion

    A polyatomic anion that contains one or more oxygen atoms. (Section 2.8)

  • rate-determining step

    The sloweststep in a multistep reaction which determines the rate of the reaction.

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • Substitution

    A reaction in which an atom or group of atoms in a compound is replaced by another atom or group of atoms.

  • terminal alkynes

    Compounds with the following structure: R!C#C!H

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

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