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Solutions for Chapter 10: U s i n g N M R S p e c t r o s c o p y t o D e d u c e S t r u c t u r e

Organic Chemistry, | 6th Edition | ISBN: 9781429204941 | Authors: K. Peter C. Vollhardt Neil E. Schore

Full solutions for Organic Chemistry, | 6th Edition

ISBN: 9781429204941

Organic Chemistry, | 6th Edition | ISBN: 9781429204941 | Authors: K. Peter C. Vollhardt Neil E. Schore

Solutions for Chapter 10: U s i n g N M R S p e c t r o s c o p y t o D e d u c e S t r u c t u r e

Solutions for Chapter 10
4 5 0 430 Reviews
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Textbook: Organic Chemistry,
Edition: 6
Author: K. Peter C. Vollhardt Neil E. Schore
ISBN: 9781429204941

This textbook survival guide was created for the textbook: Organic Chemistry,, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 10: U s i n g N M R S p e c t r o s c o p y t o D e d u c e S t r u c t u r e includes 42 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9781429204941. Since 42 problems in chapter 10: U s i n g N M R S p e c t r o s c o p y t o D e d u c e S t r u c t u r e have been answered, more than 14542 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • Anti stereoselectivity

    The addition of atoms or groups of atoms to opposite faces of a carbon-carbon double bond.

  • Chain length

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

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • E2

    A bimolecular b-elimination reaction.

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • free radical

    A substance with one or more unpaired electrons. (Section 21.9)

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • galvanic cell

    See voltaic cell. (Section 20.3)

  • heat of combustion

    The heat given off during a reaction in which an alkane reacts with oxygen to produce CO2 and water.

  • Messenger RNA (mRNA)

    A ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins

  • polar molecule

    A molecule that possesses a nonzero dipole moment. (Section 8.4)

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • saturated solution

    A solution in which undissolved solute and dissolved solute are in equilibrium. (Section 13.2)

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

  • SI units

    The preferred metric units for use in science. (Section 1.4)

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • spin-spin splitting

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms, in which the multiplicity of each signal is affected by the other.

  • termolecular

    For mechanisms, a step that involves three chemical entities.

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