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Solutions for Chapter 3.17SE: 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 3.17SE

Solutions for Chapter 3.17SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.17SE includes 2 full step-by-step solutions. Since 2 problems in chapter 3.17SE have been answered, more than 246022 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • addition reaction.

    A reaction in which one molecule adds to another. (24.2)

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • androgens

    Male sex hormones.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • catenation.

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

  • combination reaction.

    A reaction in which two or more substances combine to form a single product. (4.4)

  • empirical formula

    A chemical formula that shows the kinds of atoms and their relative numbers in a substance in the smallest possible whole-number ratios. (Section 2.6)

  • enantiomers

    Two mirror-image molecules of a chiral substance. The enantiomers are nonsuperimposable. (Section 23.4)

  • Enantiotopic groups

    Atoms or groups on an atom that give a chiral center when one of the groups is replaced by another group. A pair of enantiomers results. The hydrogens of the CH2 group of ethanol, for example, are enantiotopic. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol. Enantiotopic groups have identical chemical shifts in achiral environments but different chemical shifts in chiral environments.

  • ferromagnetism

    A form of magnetism in which unpaired electron spins align parallel to one another. (Section 23.1)

  • glycoside

    An acetal that is obtained by treating the cyclic hemiacetal form of a monosaccharide with an alcohol under acid-catalyzed conditions.

  • ion

    Electrically charged atom or group of atoms (polyatomic ion); ions can be positively or negatively charged, depending on whether electrons are lost (positive) or gained (negative) by the atoms. (Section 2.7)

  • Peptide bond

    The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid

  • Plastic

    A polymer that can be molded when hot and retains its shape when cooled

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • radical

    A chemical entity with an unpaired electron.

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

  • steric number

    The total of (single bonds + lone pairs) for an atom in a compound.

  • Transesterifi cation

    Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.

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