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Solutions for Chapter 4.1: CisTrans Isomers Result from Restricted Rotation

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 4.1: CisTrans Isomers Result from Restricted Rotation

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780134042282. Since 6 problems in chapter 4.1: CisTrans Isomers Result from Restricted Rotation have been answered, more than 30936 students have viewed full step-by-step solutions from this chapter. Chapter 4.1: CisTrans Isomers Result from Restricted Rotation includes 6 full step-by-step solutions.

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.

  • alpha 1A2 helix

    A protein structure in which the protein is coiled in the form of a helix with hydrogen bonds between C “O and N ¬H groups on adjacent turns. (Section 24.7)

  • band gap

    The energy gap between a fully occupied band called a valence band and an empty band called the conduction band. (Section 12.7)

  • catenation.

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

  • Chain propagation

    A step in a chain reaction characterized by the reaction of a reactive intermediate and a molecule to give a new reactive intermediate and a new molecule.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • covalent bond.

    A bond in which two electrons are shared by two atoms. (9.4)

  • dash

    In bond-line structures, agroup going behind the page.

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • homolitic bond cleavage

    Bond breaking that results in the formation of unchanged species called radicals.

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • molar mass

    The mass of one mole of a substance in grams; it is numerically equal to the formula weight in atomic mass units. (Section 3.4)

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • SN2 reaction

    A bimolecular nucleophilic substitution reaction.

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • spectator ions

    Ions that go through a reaction unchanged and that appear on both sides of the complete ionic equation. (Section 4.2)

  • sterically hindered

    A compound or region of a compound that is very bulky.

  • tertiary

    A term used to indicate that exactly three alkyl groups are attached directly to a particular position. For example, a tertiary carbocation has three alkyl groups attached directly to the electrophilic carbon atom (C+).

  • thioacetal

    A compound that contains two SR groups, both of which are connected to the same carbon atom.

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