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Solutions for Chapter 15.4: Preparation of Alcohols from Epoxides

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 15.4: Preparation of Alcohols from Epoxides

Solutions for Chapter 15.4
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Chapter 15.4: Preparation of Alcohols from Epoxides includes 1 full step-by-step solutions. Since 1 problems in chapter 15.4: Preparation of Alcohols from Epoxides have been answered, more than 7270 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • Alcohol

    A compound containing an !OH (hydroxyl) group bonded to a carbon atom

  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • bond length.

    The distance between the nuclei of two bonded atoms in a molecule. (9.4)

  • Brønsted-Lowry acid

    A proton donor

  • element

    A substance consisting of atoms of the same atomic number. Historically defined as a substance that cannot be separated into simpler substances by chemical means. (Sections 1.1 and 1.2)

  • globular proteins

    Proteins that consist of chains that are coiled into compact shapes.

  • glucose

    A polyhydroxy aldehyde whose formula is CH2OH1CHOH24CHO; it is the most important of the monosaccharides. (Section 24.8)

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • mass percentage

    The number of grams of solute in each 100 g of solution. (Section 13.4)

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • paramagnetism

    A property that a substance possesses if it contains one or more unpaired electrons. A paramagnetic substance is drawn into a magnetic field. (Section 9.8)

  • Photolysis

    Cleavage by light.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • radionuclide

    A radioactive nuclide. (Section 21.1)

  • tosylate

    An excellent leaving group (OTs). transition state (Sect. 6.6): A state through which a reaction passes. On an energy diagram, a transition state corresponds with a local maximum.

  • wavenumber

    In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.

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