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Solutions for Chapter 19.9SE: 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 19.9SE

Solutions for Chapter 19.9SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 19.9SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 19.9SE have been answered, more than 67667 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

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

    A reaction that occurs when an aldehyde or ketone is attacked by an enolate ion. The product of an aldol addition reaction is always a b-hydroxy aldehyde or ketone.

  • alkyl group

    A group that is formed by removing a hydrogen atom from an alkane. (Section 25.3)

  • alpha (a) helix

    For proteins, a feature of secondary structure that forms when a portion of the protein twists into a spiral.

  • amalgam.

    An alloy of mercury with another metal or metals. (21.2)

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • chirality center

    A tetrahedral carbon atom bearing four different groups.

  • Diastereotopic groups

    Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions

  • 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 shell

    A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)

  • Energy

    The ability to do work.

  • heat of combustion

    The heat given off during a reaction in which an alkane reacts with oxygen to produce CO2 and water.

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • hydrophilic

    A polar group that has favorable interactions with water.

  • ideal gas

    A hypothetical gas whose pressure, volume, and temperature behavior is completely described by the ideal-gas equation. (Section 10.4)

  • Michael acceptor

    The electrophile in a Michael reaction.

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • polarization

    For light, the orientation of the electric field.

  • soluble

    A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.

  • Strecker synthesis

    A synthetictechnique for preparing racemic a-amino acidsfrom aldehydes.

Textbook Survival Guides

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