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Solutions for Chapter 19.9: reactions of aldehydes and Ketones with GriGnard and related reaGents

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 19.9: reactions of aldehydes and Ketones with GriGnard and related reaGents

Solutions for Chapter 19.9
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Chapter 19.9: reactions of aldehydes and Ketones with GriGnard and related reaGents includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 19.9: reactions of aldehydes and Ketones with GriGnard and related reaGents have been answered, more than 36126 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • alkane

    A hydrocarbon that lacks p bonds.

  • beta particles.

    See beta rays.

  • chelate effect

    The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)

  • chlor-alkali process.

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

  • Clemmensen reduction

    A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.

  • complex lipid

    A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

  • condensation polymer

    A polymer,that is formed via a condensation reaction.

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • displacement reaction

    A reaction in which an element reacts with a compound, displacing an element from it. (Section 4.4)

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • equilibrium

    For a reaction, a state in which there is no longer an observable change in the concentrations of reactants and products.

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • homopolymer

    A polymer constructed from a single type of monomer.

  • interhalogens

    Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)

  • kinetic-molecular theory

    A set of assumptions about the nature of gases. These assumptions, when translated into mathematical form, yield the ideal-gas equation. (Section 10.7)

  • polyatomic ion

    An electrically charged group of two or more atoms. (Section 2.7)

  • rad

    A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)

  • Wavelength (l)

    The distance between consecutive peaks on a wave

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