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Solutions for Chapter 8: Reactions of Alkenes

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9780321971371

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Solutions for Chapter 8: Reactions of Alkenes

Solutions for Chapter 8
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Textbook: Organic Chemistry
Edition: 9
Author: Leroy G. Wade, Jan W. Simek
ISBN: 9780321971371

Since 89 problems in chapter 8: Reactions of Alkenes have been answered, more than 47421 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Organic Chemistry was written by and is associated to the ISBN: 9780321971371. Chapter 8: Reactions of Alkenes includes 89 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • Base peak

    The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • conformation

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

  • d sugar

    A carbohydrate for whichthe chirality center farthest from the carbonylgroup will have an OH group pointing to theright in the Fischer projection.

  • dash

    In bond-line structures, agroup going behind the page.

  • epoxide

    A cyclic ether containing a three-membered ring system. Also called an oxirane (also see Sect. 14.7).

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • glycogen

    The general name given to a group of polysaccharides of glucose that are synthesized in mammals and used to store energy from carbohydrates. (Section 24.7)

  • leaving group

    A group capable ofseparating from a compound.

  • octet rule

    A rule stating that bonded atoms tend to possess or share a total of eight valence-shell electrons. (Section 8.1)

  • oxirane

    A cyclic ether containing a three-membered ring system. Also called an epoxide.

  • physical changes

    Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • rate law

    An equation that relates the reaction rate to the concentrations of reactants (and sometimes of products also). (Section 14.3)

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • solution

    A mixture of substances that has a uniform composition; a homogeneous mixture. (Section 1.2)

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