Solutions for Chapter 24: Organic Chemistry 7th Edition

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781269406772

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 24

Solutions for Chapter 24
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9781269406772

Chapter 24 includes 52 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781269406772. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Since 52 problems in chapter 24 have been answered, more than 109949 students have viewed full step-by-step solutions from this chapter.

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

    A substance that yields hydrogen ions (H1) when dissolved in water. (2.7)

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • combustion reaction.

    A reaction in which a substance reacts with oxygen, usually with the release of heat and light, to produce a flame. (4.4)

  • coordination number.

    In a crystal lattice it is defined as the number of atoms (or ions) surrounding an atom (or ion) (11.4). In coordination compounds it is defined as the number of donor atoms surrounding the central metal atom in a complex. (23.3)

  • covalent bond

    A bond that results when two atoms share a pair of electrons.

  • crossed Claisen condensation

    A Claisen condensation reaction that occurs between different partners.

  • curved arrows

    Tools that are used for drawing resonance structures and for showing the flow of electron density during each step of a reaction mechanism.

  • Diastereotopic groups

    Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • hydrofluorocarbons (HFCs)

    Compounds that contain only carbon, fluorine, and hydrogen (no chlorine).

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • Kiliani-Fischer synthesis

    A process by which the chain of a carbohydrate is lengthened by one carbon atom.

  • observed rotation

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

  • off-resonance decoupling

    In NMR spectroscopy, a technique in which only the one-bond couplings are observed. CH3 groups appear as quartets, CH2 groups appear as triplets, CH groups appear as doublets, and quaternary carbon atoms appear as singlets.

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • Organic synthesis

    A series of reactions by which a set of organic starting materials is converted to a more complicated structure.

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • polyprotic acid

    A substance capable of dissociating more than one proton in water; H2SO4 is an example. (Section 16.6)

  • primary alkyl halide

    An organohalide in which the alpha (a) position is connected to only one alkyl group.

  • structural proteins

    Fibrous proteins that are used for their structural rigidity. Examples include a-keratins found in hair, nails, skin, feathers, and wool.

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