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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 56827 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
  • addition reaction.

    A reaction in which one molecule adds to another. (24.2)

  • alpha particles.

    See alpha rays.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • beta particles

    Energetic electrons emitted from the nucleus, symbol 0-1e or b-. (Section 21.1)

  • degenerate

    Having the same energy.

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • heat

    The flow of energy from a body at higher temperature to one at lower temperature when they are placed in thermal contact. (Section 5.1)

  • ionic compound

    A compound composed of cations and anions. (Section 2.7)

  • isomers

    Compounds whose molecules have the same overall composition but different structures. (Sections 2.9 and 23.4)

  • Ketose

    A monosaccharide containing a ketone group.

  • oxidation state

    A method of electron book-keeping in which all bonds are treated as if they were purely ionic.

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • phospholipids

    Esterlike derivatives of phosphoric acid.

  • photon

    The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)

  • Quantum mechanics

    The branch of science that studies the interaction of matter and radiation.

  • salinity

    A measure of the salt content of seawater, brine, or brackish water. It is equal to the mass in grams of dissolved salts present in 1 kg of seawater. (Section 18.3)

  • saturated

    A compound that contains no p bonds.

  • Step-growth polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers as, for example, between adipic acid and hexamethylenediamine to form nylon 66. Also called condensation polymerization.

  • steric number

    The total of (single bonds + lone pairs) for an atom in a compound.

  • strong activators

    Groups that strongly activate an aromatic ring toward electrophilic aromatic substitution, thereby significantly enhancing the rate of the reaction.