Solutions for Chapter 10.13: Retrosynthetic Analysis and the DielsAlder Reaction

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 10.13: Retrosynthetic Analysis and the DielsAlder Reaction

Solutions for Chapter 10.13
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 10.13: Retrosynthetic Analysis and the DielsAlder Reaction includes 2 full step-by-step solutions. Since 2 problems in chapter 10.13: Retrosynthetic Analysis and the DielsAlder Reaction have been answered, more than 12590 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • alkali metals

    Members of group 1A in the periodic table. (Section 7.7)

  • alpha (a) rays.

    Helium ions with a positive charge of 12. (2.2)

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • chelating agent

    A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)

  • chirality center

    A tetrahedral carbon atom bearing four different groups.

  • condensation polymer

    A polymer,that is formed via a condensation reaction.

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • diffusion

    The spreading of one substance through a space occupied by one or more other substances. (Section 10.8)

  • Enantiomers

    Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • Glycoside

    A carbohydrate in which the !OH on its anomeric carbon is replaced by !OR

  • Line-angle formula

    An abbreviated way to draw structural formulas in which vertices and line endings represent carbons

  • Pauli exclusion principle

    The rule that states that an atomic orbital or molecular orbital can accommodate a maximum of two electrons with opposite spin.

  • Primary structure of proteins

    The sequence of amino acids in the polypeptide chain, read from the N-terminal amino acid to the C-terminal amino acid.

  • property

    A characteristic that gives a sample of matter its unique identity. (Section 1.1)

  • sp2 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and two 2p atomic orbitals.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Thermochemistry

    The study of the energy of chemical structures.

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