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Solutions for Chapter 5: Thermochemistry

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Full solutions for Chemistry: The Central Science | 12th Edition

ISBN: 9780321696724

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Solutions for Chapter 5: Thermochemistry

Solutions for Chapter 5
4 5 0 303 Reviews
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Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

This expansive textbook survival guide covers the following chapters and their solutions. Since 119 problems in chapter 5: Thermochemistry have been answered, more than 201414 students have viewed full step-by-step solutions from this chapter. Chapter 5: Thermochemistry includes 119 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321696724.

Key Chemistry Terms and definitions covered in this textbook
  • (n 1 1) rule

    If a hydrogen has n hydrogens nonequivalent to it but equivalent among themselves on the same or adjacent atom(s), its 1 H!NMR signal is split into (n 1 1) peaks

  • acetal

    A functional group characterized by two alkoxy (OR) groups connected to the same carbon atom.Acetals can be used as protecting groups for aldehydes or ketones.

  • acidic oxide (acidic anhydride)

    An oxide that either reacts with a base to form a salt or with water to form an acid. (Section 22.5)

  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • Bicycloalkane

    An alkane containing two rings that share two carbons

  • bond polarity

    A measure of the degree to which the electrons are shared unequally between two atoms in a chemical bond. (Section 8.4)

  • branched polymer

    A polymer that contains a large number of branches connected to the main chain of the polymer.

  • Crystalline domain

    An ordered crystalline region in the solid state of a polymer. Also called a crystallite.

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • Hammond’s postulate

    The structure of the transition state for an exothermic step looks more like the reactants of that step than the products. Conversely, the structure of the transition state for an endothermic step looks more like the products of that step than the reactants.

  • heat

    The flow of energy from a body at higher temperature to one at lower temperature when they are placed in thermal contact. (Section 5.1)

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • oxidation

    A process in which a substance loses one or more electrons. (Section 4.4)

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • phosphatidic acid

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

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • Pro-R-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an R confi guration

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

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