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Solutions for Chapter 2.19: Sources of Alkanes and Cycloalkanes

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 2.19: Sources of Alkanes and Cycloalkanes

Solutions for Chapter 2.19
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Since 1 problems in chapter 2.19: Sources of Alkanes and Cycloalkanes have been answered, more than 34464 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 2.19: Sources of Alkanes and Cycloalkanes includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • activated complex.

    The species temporarily formed by the reactant molecules as a result of the collision before they form the product. (13.4)

  • aldol condensation

    An aldol addition followed by dehydration to give an a,bunsaturated ketone or aldehyde.

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • blocking group

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

  • C terminus

    For a peptide chain,the end that contains the COOH group. carbinolamine (Sect. 20.6): A compound containing a hydroxyl group (OH) and a nitrogen atom, both of which are connceted to the same carbon atom.

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • Carboxylic acid

    A compound containing a carboxyl, !COOH, group.

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • Clemmensen reduction

    Reduction of the C"O group of an aldehyde or ketone to a CH2 group using Zn(Hg) and HCl

  • complex ion.

    An ion containing a central metal cation bonded to one or more molecules or ions. (16.10)

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • Elastomer

    A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.

  • f-block metals

    Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)

  • heat of fusion

    The enthalpy change, ?H, for melting a solid. (Section 11.4)

  • imine

    A compound containing a CRN bond.

  • leaving group

    A group capable ofseparating from a compound.

  • molecular geometry

    The arrangement in space of the atoms of a molecule. (Section 9.2)

  • oxonium ion

    An intermediate with a positively charged oxygen atom.

  • Transesterifi cation

    Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.

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