Solutions for Chapter 16.5SE: 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 16.5SE

Solutions for Chapter 16.5SE
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Chapter 16.5SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 16.5SE have been answered, more than 108486 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.

Key Chemistry Terms and definitions covered in this textbook
  • alcohol

    An organic compound obtained by substituting a hydroxyl group 1¬OH2 for a hydrogen on a hydrocarbon. (Sections 2.9 and 24.4)

  • alkali metals.

    The Group 1A elements (Li, Na, K, Rb, Cs, and Fr). (2.4)

  • Alkaloid

    A basic nitrogen-containing compound of plant origin, many of which are physiologically active when administered to humans.

  • bonding molecular orbital.

    A molecular orbital that is of lower energy and greater stability than the atomic orbitals from which it was formed. (10.6)

  • chair conformation

    The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered.

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • Eclipsed conformation

    A conformation about a carboncarbon single bond in which the atoms or groups on one carbon are as close as possible to the atoms or groups on an adjacent carbon.

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • Excited state

    A state of a system at higher energy than the ground state.

  • Gabriel synthesis

    A method forpreparing primary amines that avoids formation of secondary and tertiary amines.

  • gas constant (R)

    The constant of proportionality in the ideal-gas equation. (Section 10.4)

  • hydroxyl group

    An OH group.

  • 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)

  • Kinetic control

    Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • Leaving group

    The group that is displaced in a substitution reaction or the Lewis base that is lost in an elimination reaction

  • Photodynamic therapy

    Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.

  • pi 1P2 molecular orbital

    A molecular orbital that concentrates the electron density on opposite sides of an imaginary line that passes through the nuclei. (Section 9.8)

  • pyrimidine

    A compound that is similar in structure to pyridine but contains one extra nitrogen atom at the 3 position.

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

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