Solutions for Chapter 2.7SE: 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 2.7SE

Solutions for Chapter 2.7SE
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Chapter 2.7SE includes 2 full step-by-step solutions. 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 2 problems in chapter 2.7SE have been answered, more than 146237 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • activity

    The decay rate of a radioactive material, generally expressed as the number of disintegrations per unit time. (Section 21.4)

  • alcohol.

    An organic compound containing the hydroxyl group —OH. (24.4)

  • Alkaloid

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

  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • base.

    A substance that yields hydroxide ions (OH2) when dissolved in water. (2.7)

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • Chain termination

    A step in a chain reaction that involves destruction of reactive intermediates

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • colloids (colloidal dispersions)

    Mixtures containing particles larger than normal solutes but small enough to remain suspended in the dispersing medium. (Section 13.6)

  • Curved arrow

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

  • ether

    A compound with the structure R!O!R.

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • Hyperconjugation

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

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • Michael donor

    The nucleophile in a Michael reaction.

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • Oxidation

    The loss of electrons. Alternatively, either the loss of hydrogens, the gain of oxygens, or both.

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • resonance structures (resonance forms)

    Individual Lewis structures in cases where two or more Lewis structures are equally good descriptions of a single molecule. The resonance structures in such an instance are “averaged” to give a more accurate description of the real molecule. (Section 8.6)

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