Solutions for Chapter 9.7SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 9.7SE

Solutions for Chapter 9.7SE
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Since 2 problems in chapter 9.7SE have been answered, more than 148594 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 9.7SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • Claisen condensation

    A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.

  • Clemmensen reduction

    A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • Disaccharide

    A carbohydrate containing two monosaccharide units joined by a glycosidic bond.

  • electrolyte

    A solute that produces ions in solution; an electrolytic solution conducts an electric current. (Section 4.1)

  • electron capture

    A mode of radioactive decay in which an inner-shell orbital electron is captured by the nucleus. (Section 21.1)

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • Infrared active

    Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • phosphatidic acid

    A phosphoric monoester, which is the simplest kind of phosphoglyceride.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • 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+).

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • syn addition

    An addition reaction in which two groups are added to the same face of a p bond.

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