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Solutions for Chapter 3: Stereoisomerism and Chirality

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 3: Stereoisomerism and Chirality

Solutions for Chapter 3
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Chapter 3: Stereoisomerism and Chirality includes 36 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 36 problems in chapter 3: Stereoisomerism and Chirality have been answered, more than 56567 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • Anti conformation

    A conformation about a single bond in which two groups on adjacent carbons lie at a dihedral angle of 180°.

  • beta sheet

    A structural form of protein in which two strands of amino acids are hydrogen-bonded together in a zipperlike configuration. (Section 24.7)

  • Bicycloalkane

    An alkane containing two rings that share two carbons

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • catenation.

    The ability of the atoms of an element to form bonds with one another. (22.3)

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • critical pressure (Pc).

    The minimum pressure necessary to bring about liquefaction at the critical temperature. (11.8)

  • delocalization

    The spreading of a charge or lone pair as described by resonance theory.

  • double helix

    The structure for DNA that involves the winding of two DNA polynucleotide chains together in a helical arrangement. The two strands of the double helix are complementary in that the organic bases on the two strands are paired for optimal hydrogen bond interaction. (Section 24.10)

  • heat capacity

    The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)

  • Infrared (IR) spectroscopy

    A spectroscopic technique in which a compound is irradiated with infrared radiation, absorption of which causes covalent bonds to change from a lower vibration state to a higher one. Infrared spectroscopy is particularly valuable for determining the kinds of functional groups present in a molecule.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • living polymer

    A polymer that isformed via anionic polymerization.

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • sigma complex

    The positively charged intermediate of an electrophilic aromatic substitution reaction.

  • Substitution

    A reaction in which an atom or group of atoms in a compound is replaced by another atom or group of atoms.

  • Thermoplastic

    A polymer that can be melted and molded into a shape that is retained when it is cooled.

  • Vinylic carbocation

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