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Solutions for Chapter Chapter 6: Alkyl Halides: Nucleophilic Substitution and Elimination

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321811394

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Solutions for Chapter Chapter 6: Alkyl Halides: Nucleophilic Substitution and Elimination

Solutions for Chapter Chapter 6
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Textbook: Organic Chemistry
Edition: 8
Author: L.g. Wade, Jr.
ISBN: 9780321811394

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Chapter Chapter 6: Alkyl Halides: Nucleophilic Substitution and Elimination includes 76 full step-by-step solutions. Since 76 problems in chapter Chapter 6: Alkyl Halides: Nucleophilic Substitution and Elimination have been answered, more than 4647 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321811394.

Key Chemistry Terms and definitions covered in this textbook
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    One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)

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    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • cation.

    An ion with a net positive charge. (2.5)

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    A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.

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    In electrocyclic reactions,a type of rotation in which the orbitals being used to form the new s bond must rotate in the same way.

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    Alkanes whose carbon atoms are joined in rings. (24.2)

  • E1

    A unimolecular b-elimination reaction

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  • Fishhook arrow

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  • High-resolution mass spectrometry

    Instrumentation that is capable of separating ions that differ in mass by as little as 0.0001 amu

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • metallic hydrides

    Compounds formed when hydrogen reacts with transition metals; these compounds contain the hydride ion, H-. (Section 22.2)

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • R

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A clockwise sequence for 1-2-3 is designated as R.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • Thermochemistry

    The study of the energy of chemical structures.

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