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Solutions for Chapter 11.7: Nucleophilic Substitution Reactions of Epoxides

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 11.7: Nucleophilic Substitution Reactions of Epoxides

This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 11.7: Nucleophilic Substitution Reactions of Epoxides includes 7 full step-by-step solutions. Since 7 problems in chapter 11.7: Nucleophilic Substitution Reactions of Epoxides have been answered, more than 41715 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • allylic bromination

    A radical reaction that achieves installation of a bromine atom at an allylic position.

  • aqueous solution

    A solution in which water is the solvent. (Chapter 4: Introduction)

  • Carboxyl group (Section 1.3D)

    A !COOH group.

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • Cis

    A prefi x meaning on the same side

  • disaccharide

    Carbohydrates comprisedof two monosaccharide units joined via aglycosidic linkage between the anomeric carbonof one monosaccharide and a hydroxyl group ofthe other monosaccharide.

  • elemental semiconductor

    A semiconducting material composed of just one element. (Section 12.7)

  • fats

    Triglycerides that are solids atroom temperature.

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Haber process

    The catalyst system and conditions of temperature and pressure developed by Fritz Haber and coworkers for the formation of NH3 from H2 and N2. (Section 15.2)

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • Organometallic compound

    A compound that contains a carbon-metal bond.

  • radial probability function

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

  • sigma 1S2 molecular orbital

    A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)

  • Vinylic carbocation

    A double-helix model for the secondary structure of a DNA molecule

  • Zaitsev’s rule

    A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond

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