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Solutions for Chapter 17.4: The Reactions of Carbonyl Compounds with Grignard Reagents

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 17.4: The Reactions of Carbonyl Compounds with Grignard Reagents

Chapter 17.4: The Reactions of Carbonyl Compounds with Grignard Reagents includes 8 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 8 problems in chapter 17.4: The Reactions of Carbonyl Compounds with Grignard Reagents have been answered, more than 41771 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymers

    Polymers that are formed via cationic addition, anionic addition, or free-radical addition.

  • alkylthio group

    An SR group.

  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • amphoteric

    Compounds that will react with either acids or bases. Amino acids are amphoteric.

  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • bond order.

    The difference between the numbers of electrons in bonding molecular orbitals and antibonding molecular orbitals, divided by two. (10.7)

  • cohesion.

    The intermolecular attraction between like molecules. (11.3)

  • combination reaction

    A chemical reaction in which two or more substances combine to form a single product. (Section 3.2)

  • common ion effect.

    The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substances. (16.2)

  • Conjugate base

    The species formed when an acid transfers a proton to a base

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • hydride ion

    An ion formed by the addition of an electron to a hydrogen atom: H-. (Section 7.7)

  • Isomers

    Different compounds with the same molecular formula.

  • Octet rule

    Group 1A–7A elements react to achieve an outer shell of eight valence electrons.

  • periodic table

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

  • Primary (1°) amine

    An amine in which nitrogen is bonded to one carbon and two hydrogens

  • primitive lattice

    A crystal lattice in which the lattice points are located only at the corners of each unit cell. (Section 12.2)

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • Spin-spin coupling

    An interaction in which nuclear spins of adjacent atoms infl uence each other and lead to the spitting of NMR signals.

  • ylide

    A compound with two oppositely charged atoms adjacent to each other.

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