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Organic Chemistry, - Standalone Book 2nd Edition - Solutions by Chapter

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Organic Chemistry, - Standalone Book | 2nd Edition - Solutions by Chapter

This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by Patricia and is associated to the ISBN: 9781118452288. Since problems from 27 chapters in Organic Chemistry, - Standalone Book have been answered, more than 18214 students have viewed full step-by-step answer. The full step-by-step solution to problem in Organic Chemistry, - Standalone Book were answered by Patricia, our top Chemistry solution expert on 01/19/18, 05:12PM. This expansive textbook survival guide covers the following chapters: 27.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymers

    Polymers that are formed via cationic addition, anionic addition, or free-radical addition.

  • Brønsted-Lowry acid

    A proton donor

  • Chain length

    The number of times the cycle of chain propagation steps repeats in a chain reaction.

  • degree of unsaturation

    The absence of two hydrogen atoms associated with a ring or a p bond.

  • Fischer esterification

    A process in which a carboxylic acid is converted into an ester when treated with an alcohol in the presence of an acid catalyst.

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • Hydration

    The addition of water.

  • hypothesis

    A tentative explanation of a series of observations or of a natural law. (Section 1.3)

  • Imine

    A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base

  • 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)

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • mole fraction

    The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • nitrous acid

    A compound with molecular formula HONO.

  • Pauli exclusion principle

    No more than two electrons may be present in an orbital. If two electrons are present, their spins must be paired

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • Reduction

    The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both

  • thermodynamics

    The study of how energy is distributed under the influence of entropy. For chemists, the thermodynamics of a reaction specifically refers to the study of the relative energy levels of reactants and products.

  • Wolff-Kishner reduction

    Reduction of the C"O group of an aldehyde or ketone to a CH2 group using hydrazine and a base. Ylide (Section 16.6)

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