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Solutions for Chapter 6: Electrophilic Additions

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 6: Electrophilic Additions

Solutions for Chapter 6
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6: Electrophilic Additions includes 49 full step-by-step solutions. Since 49 problems in chapter 6: Electrophilic Additions have been answered, more than 9940 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • alkaloids

    Naturally occurring amines isolated from plants.

  • amide

    An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)

  • basic anhydride (basic oxide)

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

  • beta emission

    A nuclear decay process where a beta particle is emitted from the nucleus; also called beta decay. (Section 21.1)

  • beta sheet

    A structural form of protein in which two strands of amino acids are hydrogen-bonded together in a zipperlike configuration. (Section 24.7)

  • bond dipole

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

  • carbonyl group

    A CRO bond. carboxylic acid derivative (Sect. 21.6): A compound that is similar in structure to a carboxylic acid (RCOOH) but the OH group of the carboxylic acid has been replaced with a different group, Z, where Z is a heteroatom such as Cl, O, N, etc. Nitriles (R!C#N) are also considered to be carboxylic acid derivatives because they have the same oxidation state as carboxylic acids.

  • closed system.

    A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)

  • Cope rearrangement

    A [3,3] sigmatropic rearrangement in which all six atoms of the cyclic transition state are carbon atoms.

  • critical pressure

    The pressure at which a gas at its critical temperature is converted to a liquid state. (Section 11.4)

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • Electron affinity

    Energy added or released when an electron is added to an atom or molecule.

  • enthalpy

    A quantity defined by the relationship H = E + PV; the enthalpy change, ?H, for a reaction that occurs at constant pressure is the heat evolved or absorbed in the reaction: ?H = qp. (Section 5.3)

  • Epoxide

    A cyclic ether in which oxygen is one atom of a three-membered ring

  • Hemiacetal

    A molecule containing an !OH and an !OR or !OAr group bonded to the same carbon

  • keto-enol tautomerization

    The equilibrium that is established between an enol and a ketone in either acid-catalyzed or basecatalyzed conditions.

  • Monosaccharide

    A carbohydrate that cannot be hydrolyzed to a simpler carbohydrate.

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • radial probability function

    The probability that the electron will be found at a certain distance from the nucleus. (Section 6.6)

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

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