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Solutions for Chapter 7: Alkenes: Structure and Reactivity

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9781305080485

Organic Chemistry | 9th Edition | ISBN: 9781305080485 | Authors: John E. McMurry

Solutions for Chapter 7: Alkenes: Structure and Reactivity

Solutions for Chapter 7
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Textbook: Organic Chemistry
Edition: 9
Author: John E. McMurry
ISBN: 9781305080485

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 7: Alkenes: Structure and Reactivity includes 75 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781305080485. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Since 75 problems in chapter 7: Alkenes: Structure and Reactivity have been answered, more than 57985 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Acetal

    A molecule containing two !OR or !OAr groups bonded to the same carbon

  • Acylium ion

    A resonance-stabilized cation with the structure [RC"O]1 or [ArC"O]1. The positive charge is delocalized over both the carbonyl carbon and the carbonyl oxygen.

  • alkylthio group

    An SR group.

  • Allylic carbon

    A carbon adjacent to a carbon-carbon double bond.

  • Axial bond

    A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.

  • base peak

    In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.

  • body-centered lattice

    A crystal lattice in which the lattice points are located at the center and corners of each unit cell. (Section 12.2)

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • dipole moment (m)

    The amount of partial charge (d ) on either end of a dipole multiplied by the distance of separation (d): m=d × d

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • intermediate

    A structure corresponding to a local minimum (valley) in an energy diagram.

  • ion-product constant

    For water, Kw is the product of the aquated hydrogen ion and hydroxide ion concentrations: 3H+43OH-4 = Kw = 1.0 * 10-14 at 25 °C. (Section 16.3)

  • ketose

    A carbohydrate that contains a ketone group.

  • Lactone

    A cyclic ester.

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • nanomaterial

    A solid whose dimensions range from 1 to 100 nm and whose properties differ from those of a bulk material with the same composition. (Section 12.1)

  • product

    A substance produced in a chemical reaction; it appears to the right of the arrow in a chemical equation. (Section 3.1)

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • syndiotactic

    A polymer in which the repeating units contain chirality centers which have alternating configuration.

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