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Solutions for Chapter 5: Stereochemistry

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Full solutions for Organic Chemistry | 11th Edition

ISBN: 9781118133576

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Solutions for Chapter 5: Stereochemistry

Solutions for Chapter 5
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Textbook: Organic Chemistry
Edition: 11
Author: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder
ISBN: 9781118133576

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 11. Since 53 problems in chapter 5: Stereochemistry have been answered, more than 40860 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781118133576. Chapter 5: Stereochemistry includes 53 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • aldol condensation

    An aldol addition followed by dehydration to give an a,bunsaturated ketone or aldehyde.

  • alkaline earth metals.

    The Group 2A elements (Be, Mg, Ca, Sr, Ba, and Ra). (2.4)

  • Celsius scale

    A temperature scale on which water freezes at 0° and boils at 100° at sea level. (Section 1.4)

  • delocalization

    The spreading of a charge or lone pair as described by resonance theory.

  • Edman degradatio

    A method for selectively cleaving and identifying the N-terminal amino acid of a polypeptide chain.

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • Ground state

    The lowest energy state of a system.

  • heterogeneous alloy

    An alloy in which the components are not distributed uniformly; instead, two or more distinct phases with characteristic compositions are present. (Section 12.3)

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • hydrophilic

    A polar group that has favorable interactions with water.

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • microstate

    The state of a system at a particular instant; one of many possible energetically equivalent ways to arrange the components of a system to achieve a particular state. (Section 19.3)

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • polypeptide

    A polymer of amino acids that has a molecular weight of less than 10,000. (Section 24.7)

  • quaternary ammonium salt

    An ionic compound containing a positively charged nitrogen atom connected to four alkyl groups.

  • 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)

  • specific rotation

    For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.

  • Thermolysis

    Cleavage by heating

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