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Solutions for Chapter 5.4: CONVERSION OF ALkENES INTO ALCOHOLS

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 5.4: CONVERSION OF ALkENES INTO ALCOHOLS

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 5.4: CONVERSION OF ALkENES INTO ALCOHOLS includes 8 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 8 problems in chapter 5.4: CONVERSION OF ALkENES INTO ALCOHOLS have been answered, more than 36770 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Aldose

    A monosaccharide containing an aldehyde group

  • alkali metals.

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

  • antibonding molecular orbital.

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

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • Aramid

    A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • deactivate

    For a substitutedaromatic ring, the effect of an electronwithdrawingsubstituent that decreases therate of electrophilic aromatic substitution.

  • deshielded

    In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is poor.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • graft copolymer

    A polymer that contains sections of one homopolymer that have been grafted onto a chain of the other homopolymer.

  • heat of combustion

    The heat given off during a reaction in which an alkane reacts with oxygen to produce CO2 and water.

  • micelle

    A group of molecules arranged in a sphere such that the surface of the sphere is comprised of polar groups, rendering the micelle water soluble.

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • nucleophile

    A compound containing an electron-rich atom that is capable of donating a pair of electrons.

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • semiconductor

    A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)

  • spontaneous process

    A process that is capable of proceeding in a given direction, as written or described, without needing to be driven by an outside source of energy. A process may be spontaneous even though it is very slow. (Section 19.1)

  • tetrahedral

    The geometry of an atom with four bonds separated from each other by 109.5°.

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