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Solutions for Chapter 2.3: CONFORmATIONS OF ALKANES

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 2.3: CONFORmATIONS OF ALKANES

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Since 4 problems in chapter 2.3: CONFORmATIONS OF ALKANES have been answered, more than 17871 students have viewed full step-by-step solutions from this chapter. Chapter 2.3: CONFORmATIONS OF ALKANES includes 4 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

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

    The product obtained from 1,4-addition across a conjugated p system.

  • alcohol

    An organic compound obtained by substituting a hydroxyl group 1¬OH2 for a hydrogen on a hydrocarbon. (Sections 2.9 and 24.4)

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • Beer’s law

    The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)

  • biodegradable polymers

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

  • blocking group

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

  • delocalization

    The spreading of a charge or lone pair as described by resonance theory.

  • Geminal coupling

    Spin-spin coupling that occurs between nonequivalent H atoms bonded to the same C atom. The H atoms are generally nonequivalent owing to restricted bond rotation in the molecule

  • Hydrogen bonding

    The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).

  • initiation

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

  • lattice vectors

    The vectors a, b, and c that define a crystal lattice. The position of any lattice point in a crystal can be represented by summing integer multiples of the lattice vectors. (Section 12.2)

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • Nitrogen rule

    A rule stating that the molecular ion of a compound with an odd number of nitrogen atoms has an odd m/z ratio; if zero or an even number of nitrogen atoms, the molecular ion has an even m/z ratio

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • oxaphosphetane

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

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • SN1

    A unimolecular nucleophilic substitution reaction.

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

  • Tesla (T)

    The SI unit for magnetic fi eld strength.

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