Concept explainers
What
(a)
Interpretation: The alkynes that forms the given ketone as the only product after hydration with
Concept introduction: A terminal alkyne reacts with
Answer to Problem 11.40P
The alkynes that forms the given ketone as the only product after hydration with
Explanation of Solution
The alkynes that forms the given ketone as the only product after hydration with
Figure 1
The terminal alkynes,
The alkynes that forms the given ketone as the only product after hydration with
(b)
Interpretation: The alkynes that forms the given ketone as the only product after hydration with
Concept introduction: A terminal alkyne reacts with
Answer to Problem 11.40P
The alkyne that forms the given ketone as the only product after hydration with
Explanation of Solution
The alkyne that forms the given ketone as the only product after hydration with
Figure 2
The terminal alkyne, ethynylcyclohexane reacts with the reagents
The alkyne that forms the given ketone as the only product after hydration with
(c)
Interpretation: The alkynes that forms the given ketone as the only product after hydration with
Concept introduction: A terminal alkyne reacts with
Answer to Problem 11.40P
The alkynes that forms the given ketone as the only product after hydration with
Explanation of Solution
The alkynes that forms the given ketone as the only product after hydration with
Figure 3
The terminal alkynes,
The alkynes that forms the given ketone as the only product after hydration with
(d)
Interpretation: The alkynes that forms the given ketone as the only product after hydration with
Concept introduction: A terminal alkyne reacts with
Answer to Problem 11.40P
The alkynes that forms the given ketone as the only product after hydration with
Explanation of Solution
The alkynes that forms the given ketone as the only product after hydration with
Figure 4
The terminal alkynes,
The alkynes that forms the given ketone as the only product after hydration with
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Chapter 11 Solutions
Organic Chemistry-Package(Custom)
- Which of the following alkenes results in the most exothermic reaction when hydrogenated with H₂ and a Pt metal catalyst to produce compound W? W an hoarrow_forwardGive the structure of ONE product formed when each of the following molecules above is chlorinated in the presence of AlCl3 Give the names of A, B, C, & Darrow_forwardWhen one mol alkene treated with an acidic KMNO4 one mol 1,2 butanedione and two mole of CO2 obtained. Please write the structure of the alkene. 2 CO2arrow_forward
- When we have discussed the enol-keto tautomerization of ketones in class, the isomerization has been facililated by an acid or base catalyst, with most ketones heavily favoring the carbonyl isomer at equilibrium. However, samples of the ketone below in its pure form (with no acid, base or water present) contain nearly 10% of the enol form! OH -90% -10% From this data, we can infer that the enol isomer of this ketone is particularly stable. Explain the stability of this enol, using terms and ideas that we have discussed in this unit.arrow_forwardDo not give handwriting solution.arrow_forwardHw.184. Provide the major organic product in the reaction below: 1) Methyl-1,2-cyclopentene oxide addition of HBrarrow_forward
- Compounds A, B, and C have the same molecular formula C4H8. They all react wotu H2/PtO2 to give the same compound. The reaction of A or B with H2O/H2SO4 or with BH3-THF, followed by treatment with a basic solution of hydrogen peroxide, gives the same compound, namely D. The reaction of C with H2O/H2SO4 also gives D. However, the reaction of C with BH3-THF, followed by HO-, H2O2 gives a new compound, E. Provide the identity of A, B, C, D, and E along with explanations of reactivity.arrow_forwardThe nitro groups on the benzene ring in the reactant serve two purposes.One is to let you know what atoms in the reactant correspond to what atomsin the product. But what role do the nitro groups play electronically – whywould the reaction be much slower if these nitro groups weren’t attached tothose benzene carbons? Draw any relevant structures to support youranswer.arrow_forward9. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) (b) (c) (d) by Br or Br H Br H OH = OHarrow_forward
- Which of these alkyl chlorides undergoes dehydrohalogenation in the presence of a strong base to give pent-2-ene (shown below) as the only alkene product? O l-chloro-2-methylbutane O 2-chloropentane O 3-chloropentane O 1-chloropentane O l-chloro-3-methylbutanearrow_forwardWrite the necessary reactants (a, c, and e) or the major product (b, d, f, and g) on the following reactions "NH₂ IFarrow_forwardThe structure below is the cyclic ether (epoxide), butene oxide: (1) CH3CH₂ -CH₂ butene oxide How could this compound be prepared from but-1-ene? Explain why butene oxide is much more reactive than its isomer, tetrahydrofuran, which is also a cyclic ether: H₂C-CH₂ H₂C CH₂ tetrahydrofuran Illustrate how butene oxide reacts with ammonia, showing details of the mechanism leading to the final product, C4H11 NO.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning