Concept explainers
a)
Interpretation:
The alkyne which can be used as a starting material for preparing methyl-n-propyl ketone is to be stated.
Concept introduction:
Addition of water to triple bonds occurs to yield an enol initially as the product. The enol then tautomerizes to give a ketone as the final product. Terminal
To state:
The alkyne which can be used as a starting material for preparing methyl-n-propyl ketone.
b)
Interpretation:
The alkyne which can be used as a starting material for preparing diethyl ketone is to be stated.
Concept introduction:
Addition of water to triple bonds occurs to yield an enol initially as the product. The enol tautomerizes to give a ketone as the final product. Terminal
To state:
The alkyne which can be used as a starting material for preparing diethyl ketone.
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Chapter 9 Solutions
Organic Chemistry
- Functional groups such as alkynes react the same in complex molecules as they do in simpler structures. The following example of alkyne reaction were taken from syntheses carried out in the research group of E. J. Corey at Harvard University. You can assume that the reactions listed involve only the alkyne, not any of the functional groups present in the molecules. Draw the expected products for the following reaction .arrow_forwardhi! could you help me with these? I could not understand what to do here. thanks!arrow_forward4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will result in the formation of an aromatic product. Then, draw the aromatic resonance product structure. Include all lone pairs in your structure. Ignore inorganic byproducts. H3O+arrow_forward
- Starting with ethyne, how could you make 2-bromopentane?arrow_forwardCCH H20, H2SO4 H9SO4 CH3 Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Hjö: -CH3 -CH3 H3O*arrow_forwardWrite the product or products that will be formed as a result of the reactions given in each line below.arrow_forward
- i cant find the answersarrow_forwardDehydration of 2-methyl-cyclopentanol followed by hydrogenation will yield which of the following products?* O 2-methylpentane O 2-methyl-2-pentene O 4 methylpentane O. methylcyclopentane O No reactionarrow_forwardThe pictured reaction shows an alkyl bromide being converted into an alkene. Choose all reagents that would produce the pictured alkene as the major product. A) NaOH/H2O B) H2O C) tBuOK/tBuOH D) EtONa/EtOHarrow_forward
- Give the product and mechanism for the following reaction. Be sure to include all mechanism arrows, lone pairs, and formal charges in your mechanism. The product is an alkene.arrow_forwardDraw structures of compounds that fit the following descriptions: a) An , unsaturated ketone, C9H8O b) An diketone c) An aromatic ketone, C9H10O d) A diene aldehyde, C7H8Oarrow_forwardfill in the blanksarrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning