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Solutions for Chapter 4.6: AddITIoN reACTIoNs oF AlKeNes

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 4.6: AddITIoN reACTIoNs oF AlKeNes

Solutions for Chapter 4.6
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Since 1 problems in chapter 4.6: AddITIoN reACTIoNs oF AlKeNes have been answered, more than 33557 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 4.6: AddITIoN reACTIoNs oF AlKeNes includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • adrenocortical hormones

    Hormones that are secreted by the cortex (the outer layer) of the adrenal glands. Adrenocortical hormones are typically characterized by a carbonyl group or hydroxyl group at C11 of the steroid skeleton.

  • Bile acid

    A cholesterol-derived detergent molecule, such as cholic acid, which is secreted by the gallbladder into the intestine to assist in the absorption of dietary lipids.

  • Brønsted acid.

    A substance capable of donating a proton. (4.3)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • coordination-sphere isomers

    Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)

  • crystal field splitting (D).

    The energy difference between two sets of d orbitals in a metal atom when ligands are present. (23.5)

  • dextrorotatory

    A compound that rotates plane-polarized light in a clockwise direction (+).

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • ground state

    The lowest-energy, or most stable, state. (Section 6.3)

  • Hofmann product

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

  • Hybridization

    The combination of atomic orbitals of different types

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • lipid

    A nonpolar molecule derived from glycerol and fatty acids that is used by organisms for long-term energy storage. (Section 24.9)

  • n+1 rule

    In NMR spectroscopy, if n is the number of neighboring protons, then the multiplicity will be n+1.

  • oxime

    A compound with the structure R2CRN!OH.

  • probability density 1c22

    A value that represents the probability that an electron will be found at a given point in space. Also called electron density. (Section 6.5)

  • protium

    The most common isotope of hydrogen. (Section 22.2)

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • rem

    A measure of the biological damage caused by radiation; rems = rads * RBE. (Section 21.9)

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

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