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Solutions for Chapter 6: The Reactions of Alkenes The Stereochemistry of Addition Reactions

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 6: The Reactions of Alkenes The Stereochemistry of Addition Reactions

Solutions for Chapter 6
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 49 problems in chapter 6: The Reactions of Alkenes The Stereochemistry of Addition Reactions have been answered, more than 35810 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Chapter 6: The Reactions of Alkenes The Stereochemistry of Addition Reactions includes 49 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Alkaloid

    A basic nitrogen-containing compound of plant origin, many of which are physiologically active when administered to humans.

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • Brønsted-Lowry base

    A compound that can serve as a proton acceptor.

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • complex lipid

    A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

  • condensation polymer

    A polymer,that is formed via a condensation reaction.

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • dehydrohalogenation

    An elimination reaction involving the loss of H and a halogen (such as Cl, Br, or I).

  • Disulfide

    A molecule containing an !S!S! group

  • Graham’s law

    A law stating that the rate of effusion of a gas is inversely proportional to the square root of its molecular weight. (Section 10.8)

  • hydrogen bonding

    A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • metathesis (exchange) reaction

    A reaction in which two substances react through an exchange of their component ions: AX + BY ¡ AY + BX. Precipitation and acid–base neutralization reactions are examples of metathesis reactions. (Section 4.2)

  • primary alkyl halide

    An organohalide in which the alpha (a) position is connected to only one alkyl group.

  • rearrangement

    One of the four arrow-pushing patterns for ionic reactions.

  • Shell

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

  • Twist-boat conformation

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

  • van der Waals radius

    The minimum distance of approach to an atom that does not cause nonbonded interaction strain.

  • Wolff-Kishner reduction

    Reduction of the C"O group of an aldehyde or ketone to a CH2 group using hydrazine and a base. Ylide (Section 16.6)

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