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Solutions for Chapter 15.4: Preparation of Alcohols from Epoxides

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 15.4: Preparation of Alcohols from Epoxides

Solutions for Chapter 15.4
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Chapter 15.4: Preparation of Alcohols from Epoxides includes 1 full step-by-step solutions. Since 1 problems in chapter 15.4: Preparation of Alcohols from Epoxides have been answered, more than 33882 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-adduct

    The product obtained from 1,4-addition across a conjugated p system.

  • alkylthio group

    An SR group.

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • buffered solution (buffer)

    A solution that undergoes a limited change in pH upon addition of a small amount of acid or base. (Section 17.2)

  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • conjugate acid-base pair.

    An acid and its conjugate base or a base and its conjugate acid. (15.1)

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • dilution

    The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • enantiotopic

    Protons that are not interchangeable by rotational symmetry but are interchangeable by reflectional symmetry.

  • Ground state

    The lowest energy state of a system.

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • Lewis base

    An electron-pair donor. (Section 16.11)

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • pressure–volume (PV) work

    Work performed by expansion of a gas against a resisting pressure. (Section 5.3)

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

  • Twist-boat conformation

    A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.

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