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Solutions for Chapter 23.11: synthesis of Amines

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 23.11: synthesis of Amines

Since 8 problems in chapter 23.11: synthesis of Amines have been answered, more than 34158 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 23.11: synthesis of Amines includes 8 full step-by-step solutions. 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.

Key Chemistry Terms and definitions covered in this textbook
  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • base peak

    In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.

  • Beer’s law

    The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)

  • buffer capacity

    The amount of acid or base a buffer can neutralize before the pH begins to change appreciably. (Section 17.2)

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • energy

    The capacity to do work or to transfer heat. (Section 5.1)

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • Molecular ion (M1)

    The radical cation formed by removal of a single electron from a parent molecule in a mass spectrometer.

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • Principle of microscopic reversibility

    This principle states that the sequence of transition states and reactive intermediates in the mechanism of any reversible reaction must be the same, but in reverse order, for the reverse reaction as for the forward reaction

  • Quaternary (4°) ammonium ion

    An ion in which nitrogen is bonded to four carbons and bears a positive charge

  • reduction

    A reaction in which a compound undergoes a decrease in oxidation state.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • soluble

    A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.

  • sp3-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with three p orbitals to form four hybridized atomic orbitals.

  • Specifi c rotation

    The observed rotation of the plane of polarized light when a sample is placed in a tube 1.0 dm in length and at a concentration of 1 g/mL for a solution. For a pure liquid, concentration is expressed in g/mL (density).

  • Valence Bond Theory

    A model of bonding that places electron pairs between adjacent atoms to create bonds.

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