Suppose the molecule below is in acidic aqueous solution. Is keto-enol tautomerization possible? • If a keto-enol tautomerization is possible, draw the mechanism for it. Be sure any extra reagents you add to the left-hand side of the first step are readily available in this solution. • If a keto-enol tautomerization is not possible, check the box under the drawing area. Add/Remove step × 5 Click and drag to start drawing a structure.
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- Consider the SN2 reaction of butyl bromide with OH- ion. CH3CH2CH2CH2B + OH- → CH3CH2CH2CH2OH + Br Assuming no other changes, what effect on the rate would result from simultaneously doubling the concentrations of both butyl bromide and the OH- ion? Draw the curved arrow mechanism for the SN1 reaction of methanol with tert-butyl iodide. Next, draw an Energy vs. Reaction Coordinate diagram for this reaction, labeling all transition states as "TS" and intermediates as appropriate for those drawn in the mechanism above, showing the relative energies on the diagram.3. Draw the systematic reaction mechanism for between the reaction of isoamyl alcohol and acetic acid. What are the products? What is the functional group of the major product? Does it have a scent? If so, what is the scent smells like?4. Charlie and Daniel wanted to make a drink containing 6.9% ethanol in the laboratory. However, there are three unlabelled reagent bottles that may contain these chemicals: ethanol, cyclohexane, and water. Devise a systematic flow chart to identify the ethanol and water in these three unlabelled reagent bottles.Assuming that the mixture in the reagent bottle containing ethanol are water and ethanol, what is the volume of the ethanol in the 132g of solution?5. Andrea and Yvette are going to cook the most delicious food that ever going to exist for their tired classmates that conducted the experiment in an organic chemistry laboratory. However, the stores are closed and they don’t have a table salt for the seasoning of their special dish so they need to…Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?
- Complete the reaction below. 1) What are the names of the starting compound and product? 2) Draw out a COMPLETE mechanism and be sure to use arrows and appropriate charges. Но на илон ля Sulfuric Acid, ???Draw the structure(s) of the organic product(s) of the Claisen condensation reaction between ethyl phenylacetate and ethyl benzoate. You do not have to consider stereochemistry. Draw only the condensation product, including the self-condensation product if applicable. Do not draw the structure of the leaving group. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C NH₂ HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one.
- Draw the curved mechanism arrows that show the deprotonation of phenol by NaOH and draw the major organic product. Draw the curved mechanism arrows that show the deprotonation of phenol by NaOH and draw the major organic product.A Suppose the molecule below is in acidic aqueous solution. Is keto-enol tautomerization possible? • If a keto-enol tautomerization is possible, draw the mechanism for it. Be sure any extra reagents you add to the left-hand side of the first step are readily available in this solution. • If a keto-enol tautomerization is not possible, check the box under the drawing area. OH 2 Add/Remove step X G Click and drag to start drawing a structure.4. Provide a synthetic route to the following molecule using benzene and cyclohexane. Reagents cannot contain more than one carbon. Provide a mechanism for the last step of your synthetic route.
- The reaction of an alkyl chloride with potassium iodide is generally carried out in acetone to maximize the amount of alkyl iodide that is formed. Why does the solvent increase the yield of alkyl iodide? (Hint: Potassium iodide is soluble in acetone, but potassium chloride is not.)Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous NextThe compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the alkyl iodide and the nucleophile that you would use. For an anionic nucleophile, you do not need to draw the counterion. Alkyl iodide: OH Draw Your Solution Nucleophile: Draw Your Solution SUPPORT