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Solutions for Chapter 6: Community

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Full solutions for Chemistry: A Molecular Approach | 3rd Edition

ISBN: 9780321809247

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Solutions for Chapter 6: Community

Solutions for Chapter 6
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Textbook: Chemistry: A Molecular Approach
Edition: 3
Author: Nivaldo J. Tro
ISBN: 9780321809247

This textbook survival guide was created for the textbook: Chemistry: A Molecular Approach, edition: 3. Chemistry: A Molecular Approach was written by and is associated to the ISBN: 9780321809247. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6: Community includes 434 full step-by-step solutions. Since 434 problems in chapter 6: Community have been answered, more than 390251 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-adduct

    The product obtainedfrom 1,2-addition across a conjugated p system.

  • Acetal

    A molecule containing two !OR or !OAr groups bonded to the same carbon

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • capillary action

    The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • 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.

  • Diels-Alder adduct

    A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.

  • electron configuration

    The arrangement of electrons in the orbitals of an atom or molecule (Section 6.8)

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • lipid

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

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • parts per billion (ppb)

    The concentration of a solution in grams of solute per 109 (billion) grams of solution; equals micrograms of solute per liter of solution for aqueous solutions. (Section 13.4)

  • Photodynamic therapy

    Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.

  • Pi (p) molecular orbital

    A molecular orbital formed by overlapping parallel 2p orbitals on adjacent atoms; its electron density lies above and below the line connecting the atoms

  • Plastic

    A polymer that can be molded when hot and retains its shape when cooled

  • Polyunsaturated fatty acid

    A fatty acid with two or more carbon-carbon double bonds in its hydrocarbon chain

  • thermoplastics

    Polymers that are hard at room temperature but soft when heated.

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

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