Solutions for Chapter 7: 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 7

Solutions for Chapter 7
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Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown
ISBN: 9780321910417

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 264 problems in chapter 7 have been answered, more than 133213 students have viewed full step-by-step solutions from this chapter. Chapter 7 includes 264 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • angstrom

    A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)

  • anti-Markovnikov addition

    An addition reaction in which a hydrogen atom is installed at the more substituted vinylic position and another group (such as a halogen) is installed at the less substituted vinylic position.

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • corrosion.

    The deterioration of metals by an electrochemical process. (18.7)

  • crystalline solid.

    A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)

  • Curved arrow

    A symbol used to show the redistribution of valence electrons in resonance contributing structures or reactions, symbolizing movement of two electrons

  • dihydroxylation

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

  • elastomers

    Polymers that return to their original shape after being stretched.

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • hydrolysis

    A reaction with water. When a cation or anion reacts with water, it changes the pH. (Sections 16.9 and 24.4)

  • Hyperconjugation

    Interaction of electrons in a s-bonding orbital with the vacant 2p orbital of an adjacent positively charged carbon.

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • oxime

    A compound with the structure R2CRN!OH.

  • sulfonate ions

    Common leaving groups. Examples include tosylate, mesylate, and triflate ions.

  • thermoplastics

    Polymers that are hard at room temperature but soft when heated.

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

  • upfield

    The right side of an NMRspectrum.

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