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Solutions for Chapter 1: Covalent Bonding and Shapes of Molecules

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 1: Covalent Bonding and Shapes of Molecules

Solutions for Chapter 1
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Since 71 problems in chapter 1: Covalent Bonding and Shapes of Molecules have been answered, more than 14095 students have viewed full step-by-step solutions from this chapter. Chapter 1: Covalent Bonding and Shapes of Molecules includes 71 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their 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
  • Aldose

    A monosaccharide containing an aldehyde group

  • alkynes

    Hydrocarbons containing one or more carbon–carbon triple bonds. (Section 24.2)

  • anti addition

    An addition reaction in which two groups are installed on opposite sides of a p bond.

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • bending

    In IR spectroscopy, a type of vibration that generally produces a signal in the fingerprint region of an IR spectrum.

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • concentration

    The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)

  • disulfide

    A compound with the structure R!S!S!R.

  • hypothesis

    A tentative explanation of a series of observations or of a natural law. (Section 1.3)

  • ketose

    A carbohydrate that contains a ketone group.

  • Lindlar catalyst

    Finely powdered palladium metal deposited on solid calcium carbonate that has been specially modifi ed with lead salts. Its particular use is as a catalyst for the reduction of an alkyne to a cis alkene

  • Orbital

    A region of space that can hold two electrons

  • pH titration curve

    A graph of pH as a function of added titrant. (Section 17.3)

  • 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)

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • secondary

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

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • Steroid

    A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.

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