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Solutions for Chapter 15.8SE: 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 15.8SE

Solutions for Chapter 15.8SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 15.8SE have been answered, more than 66508 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 15.8SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • bromohydrin

    A compound containing a Br group and a hydroxyl group (OH) on adjacent carbon atoms.

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • chlor-alkali process.

    The production of chlorine gas by the electrolysis of aqueous NaCl solution. (22.6)

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • dehydration

    An elimination reaction involving the loss of H and OH.

  • disrotatory

    In electrocyclicreactions, a type of rotation in which the orbitalsbeing used to form the new s bond must rotate in opposite directions (one rotates clockwise while the other rotates counterclockwise).

  • heat capacity

    The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)

  • High-resolution mass spectrometry

    Instrumentation that is capable of separating ions that differ in mass by as little as 0.0001 amu

  • Hydroboration-oxidation

    A method for converting an alkene to an alcohol. The alkene is treated with borane (BH3) to give a trialkylborane, which is then oxidized with alkaline hydrogen peroxide to give an alcohol

  • organohalide

    An organic compound containing at least one halogen.

  • Para (p)

    Refers to groups occupying l,4-positions on a benzene ring

  • precipitate

    An insoluble substance that forms in, and separates from, a solution. (Section 4.2)

  • Protic acid

    An acid that is a proton donor in an acidbase reaction.

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • Sigma (s) molecular orbital

    A molecular orbital in which electron density is concentrated between two nuclei, along the axis joining them, and is cylindrically symmetrical

  • thermodynamic control

    A reaction for which the ratio of products is determined solely by the distribution of energy among the products.

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

Textbook Survival Guides

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