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 5661 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 Patricia and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.

  • alkynes

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

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • bonding molecular orbital.

    A molecular orbital that is of lower energy and greater stability than the atomic orbitals from which it was formed. (10.6)

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • d sugar

    A carbohydrate for whichthe chirality center farthest from the carbonylgroup will have an OH group pointing to theright in the Fischer projection.

  • Double helix

    A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • electron-sea model

    A model for the behavior of electrons in metals. (Section 12.4)

  • enzymes

    Important biological molecules that catalyze virtually all cellular processes.

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • halogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.

  • monomers

    Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • regioselective

    A reaction that can produce two or more constitutional isomers but nevertheless produces one as the major product.

  • resonance structures

    A series of structures that are melded together (conceptually) to circumvent the inadequacies of bond-line drawings.

  • Secondary (2°) amine

    An amine in which nitrogen is bonded to two carbons and one hydrogen

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.

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