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Solutions for Chapter 2: Constitutional Isomerism in Alkanes

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 2: Constitutional Isomerism in Alkanes

Solutions for Chapter 2
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Since 58 problems in chapter 2: Constitutional Isomerism in Alkanes have been answered, more than 13227 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2: Constitutional Isomerism in Alkanes includes 58 full step-by-step solutions. 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
  • Acyl group

    An RCO! or ArCO! group.

  • antibonding MO

    A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.

  • atmospheric pressure.

    The pressure exerted by Earth’s atmosphere. (5.2)

  • bomb calorimeter

    A device for measuring the heat evolved in the combustion of a substance under constant-volume conditions. (Section 5.5)

  • cation.

    An ion with a net positive charge. (2.5)

  • common ion effect.

    The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substances. (16.2)

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • Haloarene (aryl halide)

    A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X

  • hydride shift

    A type of carbocation rearrangement that involves the migration of a hydride ion (H-).

  • Lewis base

    Any molecule or ion that can form a new covalent bond by donating a pair of electrons.

  • Lipid bilayer

    A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • Ostwald process

    An industrial process used to make nitric acid from ammonia. The NH3 is catalytically oxidized by O2 to form NO; NO in air is oxidized to NO2; HNO3 is formed in a disproportionation reaction when NO2 dissolves in water. (Section 22.7)

  • polar covalent bond

    A bond in which the difference in electronegative values of the two atoms is between 0.5 and 1.7.

  • Resonance in NMR spectroscopy

    The absorption of electromagnetic radiation by a precessing nucleus and the resulting “fl ip” of its nuclear spin from the lower energy state to the higher energy state.

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

  • syn-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 0°.

  • Triol

    A compound containing three hydroxyl groups.

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