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Solutions for Chapter 6.2SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 6.2SE

Solutions for Chapter 6.2SE
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Chapter 6.2SE includes 2 full step-by-step solutions. Since 2 problems in chapter 6.2SE have been answered, more than 65296 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Activating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.

  • alkyl group

    A group that is formed by removing a hydrogen atom from an alkane. (Section 25.3)

  • Anti conformation

    A conformation about a single bond in which two groups on adjacent carbons lie at a dihedral angle of 180°.

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • chain reaction

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

  • coordination compound.

    A neutral species containing one or more complex ions. (23.3)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • Kiliani-Fischer synthesis

    A process by which the chain of a carbohydrate is lengthened by one carbon atom.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • Newman projection

    A way to view a molecule by looking along a carbon-carbon single bond

  • Nonbonding electrons

    Valence electrons not involved in forming covalent bonds. Also called unshared pairs or lone pairs.

  • Nucleotide

    A nucleoside in which a molecule of phosphoric acid is esterifi ed with an !OH of the monosaccharide, most commonly either the 39!OH or the 59!OH.

  • Organometallic compound

    A compound that contains a carbon-metal bond.

  • peptide bond

    A bond formed between two amino acids. (Section 24.7)

  • Polymer

    From the Greek, poly 1 meros, meaning many parts. Any long-chain molecule synthesized by linking together many single parts called monomers

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • Raman spectroscopy

    A vibrational molecular spectroscopy that is complementary to infrared (IR) spectroscopy in that infrared inactive vibrations are seen in Raman spectroscopy.

  • sp2-hybridized orbitals

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

  • Torsional strain

    Strain that arises when nonbonded atoms separated by three bonds are forced from a staggered conformation to an eclipsed conformation. Torsional strain is also called eclipsed-interaction strain.

Textbook Survival Guides

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