EBK ESSENTIAL ORGANIC CHEMISTRY
EBK ESSENTIAL ORGANIC CHEMISTRY
3rd Edition
ISBN: 9780100659469
Author: Bruice
Publisher: YUZU
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Chapter 4, Problem 63P

Draw structures for each of the following:

  1. a. (S)-1-bromo-1-chlorobutane
  2. b. an achiral isomer of 1,2-dimethylcyclohexane
  3. c. a chiral isomer of 1,2-dibromocyclobutane
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36. The emission spectrum below for a one-electron (hydrogen-like) species in the gas phase shows all the lines, before they merge together, resulting from transitions to the first excited state from higher energy states. Line A has a wavelength of 434 nm. BA Increasing wavelength, λ (a) What are the upper and lower principal quantum numbers corresponding to the lines labeled A and B? (b) Identify the one-electron species that exhibits the spectrum.
f) The unusual molecule [2.2.2] propellane is pictured. 1) Given the bond length and bond angles in the image, what hybridization scheme best describes the carbons marked by the askerisks? 2) What types of orbitals are used in the bond between the two carbons marked by the askerisks? 3) How does this bond compare to an ordinary carbon-carbon bond (which is usually 1.54 Å long)? H₂C H₂C CH2 1.60Å ハ C. * CH₂ H₂C * C H₂ 120°
Question Resonance Forms a) Draw all resonance forms of the molecules. Include curved arrow notation. Label major resonance contributor Resonance Forms a) Draw all resonance forms of the molecules. Include curved arrow notation. Label major resonance contributor

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EBK ESSENTIAL ORGANIC CHEMISTRY

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