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Solutions for Chapter 3.14: Conformers of Monosubstituted Cyclohexanes

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 3.14: Conformers of Monosubstituted Cyclohexanes

Solutions for Chapter 3.14
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This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780134042282. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.14: Conformers of Monosubstituted Cyclohexanes includes 1 full step-by-step solutions. Since 1 problems in chapter 3.14: Conformers of Monosubstituted Cyclohexanes have been answered, more than 31227 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acidic cleavage

    A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.

  • Acyl group

    An RCO! or ArCO! group.

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • bond length

    The distance between the centers of two bonded atoms. (Section 8.3)

  • Circular DNA

    A type of double-stranded DNA in which the 59 and 39 ends of each strand are joined by phosphodiester groups.

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • colloids (colloidal dispersions)

    Mixtures containing particles larger than normal solutes but small enough to remain suspended in the dispersing medium. (Section 13.6)

  • compound semiconductor

    A semiconducting material formed from two or more elements. (Section 12.7)

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • hemiacetal

    A compound containing a hydroxyl group (OH) and an alkoxy group (OR) connected to the same carbon atom.

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • Infrared (IR) spectroscopy

    A spectroscopic technique in which a compound is irradiated with infrared radiation, absorption of which causes covalent bonds to change from a lower vibration state to a higher one. Infrared spectroscopy is particularly valuable for determining the kinds of functional groups present in a molecule.

  • initiation

    In radical reaction mechanisms, a step in which radicals are created.

  • Ketone

    A compound containing a carbonyl group bonded to two carbons.

  • Nucleophilic acyl substitution

    A reaction in which a nucleophile bonded to the carbon of an acyl group is replaced by another nucleophile.

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

  • Zaitsev product

    The more substituted product (alkene) of an elimination reaction.

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