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Solutions for Chapter 7.9 SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 7.9 SE

Solutions for Chapter 7.9 SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 7.9 SE have been answered, more than 177583 students have viewed full step-by-step solutions from this chapter. Chapter 7.9 SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • 1,3-diaxial interaction

    Steric interactions that occur between axial substituents in a chair conformation.

  • alkaline earth metals

    Members of group 2A in the periodic table. (Section 7.7)

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • catalyst

    A compound that can speed up the rate of a reaction without itself being consumed by the reaction.

  • double bond

    A covalent bond involving two electron pairs. (Section 8.3)

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • Graham’s law

    A law stating that the rate of effusion of a gas is inversely proportional to the square root of its molecular weight. (Section 10.8)

  • Grignard reagent

    A carbanion with the structure RMgX.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • neutralization reaction

    A reaction in which an acid and a base react in stoichiometrically equivalent amounts; the neutralization reaction between an acid and a metal hydroxide produces water and a salt. (Section 4.3)

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • Phenol

    A compound that contains an !OH bonded to a benzene ring; a benzenol.

  • progestins

    Female sex hormones.

  • rate-determining step

    The slowest elementary step in a reaction mechanism. (Section 14.6)

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules

  • SN2 reaction

    A bimolecular nucleophilic substitution reaction.

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • symmetrical ether

    An ether (R!O!R) where both R groups are identical.

  • transport protein

    A protein used to transport molecules or ions from one location to another. Hemoglobin is a classic example of a transport protein, used to transport molecular oxygen from the lungs to all the tissues of the body.

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