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Solutions for Chapter 2.15SE: 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 2.15SE

Solutions for Chapter 2.15SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 2.15SE have been answered, more than 66682 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2.15SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Acetal

    A molecule containing two !OR or !OAr groups bonded to the same carbon

  • Addition reaction

    A reaction in which two atoms or groups of atoms react with a double bond, forming a compound with the two new groups bonded to the carbons of the original double bond.

  • amphiprotic

    Refers to the capacity of a substance to either add or lose a proton 1H+2. (Section 16.2)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • branched polymer

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

  • calorimetry

    The experimental measurement of heat produced in chemical and physical processes. (Section 5.5)

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • diol

    A compound containing two hydroxyl groups (OH).

  • endothermic process

    A process in which a system absorbs heat from its surroundings. (Section 5.2)

  • Frost circle

    A graphic method for determining the relative energies of p MOs for planar, fully conjugated, monocyclic compounds.

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • Nucleophile

    From the Greek meaning nucleus-loving. Any species that can donate a pair of electrons to form a new covalent bond; alternatively, a Lewis base

  • Orthogonal

    Having no net overlap.

  • oxidation

    A reaction in which one compound undergoes an increase in oxidation state.

  • phosphatidic acid

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

  • random copolymer

    A polymer, comprised of more than one kind of repeating unit, in which there is a random distribution of repeating units.

  • replacement test

    A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • sp Hybrid orbitaL

    A hybrid atomic orbital formed by the combination of one s atomic orbital and one 2p atomic orbital.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

Textbook Survival Guides

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