Question
In: Chemistry
When 1-‐iodo-‐1-‐methylcyclohexane is treated with NaOCH2CH3 as the base, the more highly substituted alkene product predominates.When...
When 1-‐iodo-‐1-‐methylcyclohexane is treated with NaOCH2CH3 as the base, the more highly substituted alkene product predominates.When KOC(CH3)3 is used as the base, the less highly substituted alkene predominates. Give the structures of the two products and offer an explanation.
Solutions
queen_honey_blossom answered 2 years agoRelated Solutions
Give mechanism and product expected when 1-hexyne is treated with NaNH2 in liquid ammonia.
Give mechanism and product expected when 1-hexyne is treated
with NaNH2 in liquid ammonia.
1. The possible components of your mixture are unreacted ferrocene and the substituted ferrocene product(s) of...
1. The possible components of your mixture are unreacted
ferrocene and the substituted ferrocene product(s) of your
reaction, which should travel the farthest up the TLC plate
(highest Rf) and why?
2. Which should have a higher Rf value: the mono-substituted
ferrocene or the di-substituted ferrocene?
3. In the column chromatography portion of your experiment next
week, you use different solvents or solvent mixtures to elute the
column for separation of your product mixture. Why is this
required? Why use...
In acid-catalyzed addition of water to alkene, alcohol is the product.
In acid-catalyzed addition of water to alkene, alcohol is the product. The conjugate base of the acid may compete with water for the newly formed carbocation and give a different product (other than alcohol). Among the following acids, which is the best acid catalyst? Which is the worst? Depend your answers.
HOAc HCl H2SO4 CF3COOH
Why are Not for Profit investments treated differently and why would they be more scrutinized when...
Why are Not for Profit investments treated differently and why
would they be more scrutinized when compared to private
companies?
Draw a diagram that illustrates the hyperconjugation that explains these phenomena: - more substituted alkenes have...
Draw a diagram that illustrates the
hyperconjugation that explains these
phenomena:
- more substituted alkenes have lower heats of hydrogenation
- more substituted carbocations are more stable
- staggered conformations are lower in energy than eclipsed
- allylic SN2 is faster than non-allylic
Be sure to use shading to indicate the location of nodes and use
arrows to show overlap.
Thank you!!!
1) What alkene(s) will be produced when each of the following alcohols is dehydrated? 2- propanol...
1) What alkene(s) will be produced when each of the
following alcohols is dehydrated?
2- propanol
2- butanol
2) Why is phosphoric acid preferred over sulfuric acid
for dehydration of alcohols?
3) What measures should be taken if droplets of
phosphoric acid are splashed in the eyes?
4) Give an example of a skeletal rearrangement during a
dehydration experiment.
5) What is the purpose of adding anhydrous sodium
sulfate to the dehydration product in experiment B?
Identify a product that is monopolisticly competitive. Specifically, define what products it could be substituted for...
Identify a product that is monopolisticly competitive.
Specifically, define what products it could be substituted for and
also what characteristics make is differentiated from those
products. Discuss what the seller of the product could do to
increase the differentiation of that product, and
Discuss what impact increasing the differentiation of that product
would likely have on the products price and the seller's profits
earned from the product.
When ortho-bromonitrobenzene is treated with NaOH and heat one product is formed. a) show the mechanism...
When ortho-bromonitrobenzene is treated with NaOH and heat one
product is formed.
a) show the mechanism
b) would the reaction occur if starting material was
para-bromotoluene
c) would the reaction occur if starting material was
meta-bromotoluene
1. 1-methyl-1,2-epoxycyclohexane treated with 1) CH3MgBr and 2) H20 provides what product? 2. 1,5-epoxypentane treated with...
1. 1-methyl-1,2-epoxycyclohexane treated with 1) CH3MgBr and 2)
H20 provides what product?
2. 1,5-epoxypentane treated with EXCESS HI provides what
product?
What happens to a halogenation reaction of a Alkene or Alkyne when the reaction is cold?
What happens to a halogenation reaction of a Alkene or Alkyne when
the reaction is cold?
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