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Explain why a tertiary alkyl

A phosphorus ylide is a Wittig reagent and is prepared using an alkyl halide and triphenyl phosphide. Using an appropriate
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2. asked by Davepee
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Explain why the stability of alkyl carbocations is:tertiary > secondary > primary > methyl Thanks!
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2. asked by Kimberly
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Explain why a tertiary alkyl halide cannot be used to prepare an phosphorus ylide. Show the reaction mechanisms.
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2. asked by Davepee
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3 Chloro-3-methylcyclohexene could be best classified as a _____________ alkyl halide.a. Primary b. Secondary c. Tertiary d.
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2. asked by BBXcream
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Could someone answer this. Im stuck on it.In general, the most elegant way to add one carbon with an OH on it to a primary alkyl
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2. asked by Anonymous
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Please check these out for me, if I am correct:Match the following statements with SN1 or SN2 reactions: 1) The order of
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2. asked by K
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Please check these out for me, if I am correct:Match the following statements with SN1 or SN2 reactions: 1) The order of
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2. asked by K
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Elimination reactions are favored over substitution reactions when nucleophiles used are bulky and the substrate is a tertiary
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2. asked by Missy.Sippy
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Look up the density of n-butyl chloride (1-chlorobutane). Assume that this alkyl halide was prepared instead of the bromide.
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2. asked by Ariel
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5. Look up the density of n-butyl chloride (1-chlorobutane). Assume that this alkyl halide was prepared instead of the bromide.
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2. asked by Scarlet
3. 1,676 views