Chapter 12: Q-21-21-4P (page 354)
Rank the compounds in each of the following sets in order of their expected reactivity toward nucleophilic acyl substitution:
Short Answer
The order of reactivity towards nucleophilic acyl substitution:
(a)
(b)
Chapter 12: Q-21-21-4P (page 354)
Rank the compounds in each of the following sets in order of their expected reactivity toward nucleophilic acyl substitution:
The order of reactivity towards nucleophilic acyl substitution:
(a)
(b)
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How might you use IR spectroscopy to distinguish between the followingpairs of isomers?
(a) CH3 CH2 OH and CH3 OCH3
(b) Cyclohexane and 1 - hexene
(c) CH3 CH2 CO2 H and HOCH2 CH2 CHO
Question: Halogenated compounds are particularly easy to identify by their mass
spectra because both chlorine and bromine occur naturally as mixtures
of two abundant isotopes. Recall that chlorine occurs as 35Cl (75.8%)
and 37C (24.2%); and bromine occurs as 79Br (50.7%) and 81Br (49.3%).
At what masses do the molecular ions occur for the following formulas?
What are the relative percentages of each molecular ion?
(a)Bromomethane, CH3Br
(b)1-Chlorohexane, C6H13Cl
Question: 2-Methylpentane (C6H14)has the mass spectrum shown. Which peak
represents? Which is the base peak? Propose structures for fragment
ions of m/z=71, 57, 43, and 29. Why does the base peak have the mass it does?
Question: Where might the following compounds have IR absorptions?
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