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Solutions for Chapter 1.7: Structural Formulas of Organic Molecules

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 1.7: Structural Formulas of Organic Molecules

Since 3 problems in chapter 1.7: Structural Formulas of Organic Molecules have been answered, more than 37035 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 1.7: Structural Formulas of Organic Molecules includes 3 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • atomic number

    The number of protons in the nucleus of an atom of an element. (Section 2.3)

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • bimolecular reaction

    An elementary reaction that involves two molecules. (Section 14.6)

  • bond angles

    The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • carbonyl group

    A CRO bond. carboxylic acid derivative (Sect. 21.6): A compound that is similar in structure to a carboxylic acid (RCOOH) but the OH group of the carboxylic acid has been replaced with a different group, Z, where Z is a heteroatom such as Cl, O, N, etc. Nitriles (R!C#N) are also considered to be carboxylic acid derivatives because they have the same oxidation state as carboxylic acids.

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • cohesion.

    The intermolecular attraction between like molecules. (11.3)

  • Confi guration

    Refers to the arrangement of atoms about a stereocenter

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • Frequency

    The number of full cycles of a wave that pass a given point in a second, and reported in hertz (Hz), which has the units s21

  • heterogeneous catalyst

    A catalyst that is in a different phase from that of the reactant substances. (Section 14.7)

  • homopolymer

    A polymer constructed from a single type of monomer.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • l sugar

    A carbohydrate for which the chirality center farthest from the carbonyl group will have an OH group pointing to the left in the Fischer projection.

  • Line-angle formula

    An abbreviated way to draw structural formulas in which vertices and line endings represent carbons

  • silicates

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

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

  • Tertiary (3°) amine

    An amine in which nitrogen is bonded to three carbons

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

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