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Solutions for Chapter 3.13: Conformers of Cyclohexane

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 3.13: Conformers of Cyclohexane

Solutions for Chapter 3.13
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This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Since 1 problems in chapter 3.13: Conformers of Cyclohexane have been answered, more than 7194 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780134042282. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.13: Conformers of Cyclohexane includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alditol

    The product obtained when the aldehyde group of an aldose is reduced.

  • alkyl group

    A substituent lacking p bonds and comprised of only carbon and hydrogen atoms.

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • electromagnetic spectrum

    Therange of all frequencies of electromagnetic radiation,which is arbitrarily divided into severalregions, most commonly by wavelength.

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • free induction decay

    In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.

  • Hammond postulate

    In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.

  • heat of fusion

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

  • interhalogens

    Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • molarity

    The concentration of a solution expressed as moles of solute per liter of solution; abbreviated M. (Section 4.5)

  • oxidation

    A reaction in which one compound undergoes an increase in oxidation state.

  • pure substance

    Matter that has a fixed composition and distinct properties. (Section 1.2)

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • Rearrangement

    A change in connectivity of the atoms in a product compared with the con nectivity of the same atoms in the starting material.

  • s-cis

    A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).

  • Stereocenter

    An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

  • tetrahedral intermediate

    An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.

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