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Solutions for Chapter 15.11: More Examples of 1 H NMR Spectra

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 15.11: More Examples of 1 H NMR Spectra

Since 8 problems in chapter 15.11: More Examples of 1 H NMR Spectra have been answered, more than 38315 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 15.11: More Examples of 1 H NMR Spectra includes 8 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • Alkyl group

    A group derived by removing a hydrogen from an alkane; given the symbol R!

  • calorie

    A unit of energy; it is the amount of energy needed to raise the temperature of 1 g of water by 1 °C from 14.5 °C to 15.5 °C. A related unit is the joule: 1 cal = 4.184 J. (Section 5.1)

  • cell potential

    The potential difference between the cathode and anode in an electrochemical cell; it is measured in volts: 1 V = 1 J>C. Also called electromotive force. (Section 20.4)

  • Chair conformation

    The most stable nonplanar conformation of a cyclohexane ring; all bond angles are approximately 109.5°, and all bonds on adjacent carbons are staggered.

  • chromophore

    In UV-Vis spectroscopy, the region of the molecule responsible for the absorption (the conjugated p system).

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • condensation polymer

    A polymer,that is formed via a condensation reaction.

  • conjugate base

    In an acid-base reaction, the product that results when an acid is deprotonated.

  • copolymer.

    A polymer containing two or more different monomers. (25.2)

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • fuel value

    The energy released when 1 g of a substance is combusted. (Section 5.8)

  • Hammond postulate

    In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • lambda max (lmax)

    In UVVis spectroscopy, the wavelength of maximum absorption.

  • Lewis base

    A compound capable offunctioning as an electron pair donor.

  • Para (p)

    Refers to groups occupying l,4-positions on a benzene ring

  • periodic table

    The arrangement of elements in order of increasing atomic number, with elements having similar properties placed in vertical columns. (Section 2.5)

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

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