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Solutions for Chapter Lesson 33: Functional Groups

Full solutions for Living by Chemistry | 2nd Edition

ISBN: 9781464142314

Solutions for Chapter Lesson 33: Functional Groups

This expansive textbook survival guide covers the following chapters and their solutions. Chapter Lesson 33: Functional Groups includes 11 full step-by-step solutions. Since 11 problems in chapter Lesson 33: Functional Groups have been answered, more than 21659 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Living by Chemistry, edition: 2. Living by Chemistry was written by and is associated to the ISBN: 9781464142314.

Key Chemistry Terms and definitions covered in this textbook
  • asymmetric hydrogenation

    The addition of H2 across only one face of a p bond.

  • band

    An array of closely spaced molecular orbitals occupying a discrete range of energy. (Section 12.4)

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • crystal field splitting (D).

    The energy difference between two sets of d orbitals in a metal atom when ligands are present. (23.5)

  • Dalton’s law of partial pressures.

    The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)

  • E1

    A unimolecular elimination reaction.

  • elementary reaction

    A process in a chemical reaction that occurs in a single step. An overall chemical reaction consists of one or more elementary reactions or steps. (Section 14.6)

  • estrogens

    Female sex hormones.

  • hydroxyl group

    An OH group.

  • isotactic

    A polymer in which the repeating units contain chirality centers which all have the same configuration.

  • ortho

    On an aromatic ring, the C2 position.

  • oxirane

    A cyclic ether containing a three-membered ring system. Also called an epoxide.

  • ozone

    The name given to O3, an allotrope of oxygen. (Section 7.8)

  • Protecting group

    Reversibly creating an unreactive group for the purpose of preventing a functional group from potentially reacting to give an unwanted product or products

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • resolving agents

    A compound that can be used to achieve the resolution of enantiomers.

  • resonance structures (resonance forms)

    Individual Lewis structures in cases where two or more Lewis structures are equally good descriptions of a single molecule. The resonance structures in such an instance are “averaged” to give a more accurate description of the real molecule. (Section 8.6)

  • retro Diels-Alder reaction

    The reverse of a Diels-Alder reaction, achieved at high temperature. A cyclohexene derivative is converted into a diene and a dienophile.

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

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