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Solutions for Chapter 5.9: Dehydration of Alcohols

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 5.9: Dehydration of Alcohols

Solutions for Chapter 5.9
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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. Chapter 5.9: Dehydration of Alcohols includes 1 full step-by-step solutions. Since 1 problems in chapter 5.9: Dehydration of Alcohols have been answered, more than 36212 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic carbocation

    A carbocation in which an allylic carbon bears the positive charge.

  • alpha (a) helix

    For proteins, a feature of secondary structure that forms when a portion of the protein twists into a spiral.

  • Aufbau principle.

    As protons are added one by one to the nucleus to build up the elements, electrons similarly are added to the atomic orbitals. (7.9)

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • Boyle’s law.

    The volume of a fixed amount of gas maintained at constant temperature is inversely proportional to the gas pressure. (5.3)

  • chemical reactions

    Processes in which one or more substances are converted into other substances; also called chemical changes. (Section 1.3)

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • diagonal relationship.

    Similarities between pairs of elements in different groups and periods of the periodic table. (8.6)

  • Diastereomers

    Stereoisomers that are not mirror images of each other; refers to relationships among two or more objects

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • mass percentage

    The number of grams of solute in each 100 g of solution. (Section 13.4)

  • methine group

    A CH group.

  • mineral

    A solid, inorganic substance occurring in nature, such as calcium carbonate, which occurs as calcite. (Section 23.1)

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • plasticizers

    Small molecules that are trapped between polymer chains where they function as lubricants, preventing the polymer from being brittle.

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

  • Vibrational infrared region

    A common type of spin-spin coupling involving the H atoms on two C atoms that are bonded to each other.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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