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Solutions for Chapter 1.7SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 1.7SE

Solutions for Chapter 1.7SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 1.7SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 1.7SE have been answered, more than 309886 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.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.

  • amide

    An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • biodegradable polymers

    Polymers that can be broken down by enzymes produced by soil microorganisms.

  • boiling-point elevation (DTb).

    The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)

  • carboxylic acid

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

  • cell voltage.

    Difference in electrical potential between the anode and the cathode of a galvanic cell. (18.2)

  • Chromatography

    A separation method involving passing a vapor or solution mixture through a column packed with a material with different affi nities for different components of the mixture.

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • 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.

  • cycloalkanes.

    Alkanes whose carbon atoms are joined in rings. (24.2)

  • Equatorial bond

    A bond to a chair conformation of cyclohexane that extends from the ring roughly perpendicular to the imaginary axis through the center of the ring; a bond that lies roughly along the equator of a cyclohexane ring

  • London dispersion forces

    Attractive forces between transient dipole moments, observed in alkanes.

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • primary cell

    A voltaic cell that cannot be recharged. (Section 20.7)

  • Raman spectroscopy

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

  • Resonance hybrid

    A molecule, ion, or radical described as a composite of a number of contributing structures

  • Schiff base

    An alternative name for an imine

  • SN2 reaction

    A bimolecular nucleophilic substitution reaction.

  • unsaturated

    A compound containingone or more p bonds.