Chapter 18: Q4P (page 923)
Use equations to show the fragmentation leading to each numbered peak in the mass spectrum of cotane-2-one.
Short Answer
Fragmentation equations of octane-2-one
Chapter 18: Q4P (page 923)
Use equations to show the fragmentation leading to each numbered peak in the mass spectrum of cotane-2-one.
Fragmentation equations of octane-2-one
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Get started for freeShow how you would synthesize each compound from starting materials containing no more than six carbon atoms.
(a)
(b)
(c)
Hydration of alkynes (via oxymercuration) gives good yields of single compounds only with symmetrical or asymmetrical alkynes. Show what products would be from hydration fo each compound.
(a) hex-3-yne
(b) hex-2-yne
(c) hex-1-yne
(d) cyclodecyne
(e) 3-methylcyclodecyne
Show how you would accomplish the following synthetic conversions. You may use any additional reagents and solvents you need.
Propose a mechanism for both parts of the Wolff-Kishner reduction of cyclohexanone: the formation of the hydrazone, and then the base catalyzed reduction with evolution of nitrogen gas.
Two structures for the sugar glucose are shown on page 950. Interconversion of the open-chain and cyclic hemiacetal forms is catalyzed by either acid or base.
(a) Propose a mechanism for the cyclization, assuming a trace of acid is present.
(b) The cyclic hemiacetal is more stable than the open-chain form, so very little of the open-chain form is present at equilibrium. Will an aqueous solution of glucose reduce Tollens reagent and give a positive Tollens test? Explain.
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