Hepten-2-one is a ketone that also contains a C=C double bond between carbons 6 and 7. If this substrate is treated with excess (or a LOT of) H2 in the presence of Pt, Pd, or Ni metal, the major substrate product (of this one-reaction process) would be ___ .
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- For the substrate below write all possible reactions. Ethanol is a weak nucleophile. Please verify whether a hydride shift is possible. + CH3CH2OHWhat is the final product of the following reaction sequence? Give structural details of all significant intermediates.Write the main product(s) that will be formed as a result of the following reaction, together with its mechanism.
- Indicate the two most probable reagents for the following substrate/product pair. S-Identify the MAJOR product that would be obtained at the end of the following reaction sequence. (i.e. the final product not the "isolated intermediate") H NaNH2 then HCI Br isolated excess intermediateshow the missing reagents and intermediates in the reaction sequence below
- Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the structure of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. H. BH₂ BH₂ THF . Draw Major Borane Intermediate H2O2, NaOH Draw Major Productwrite down in words the necessary conditions to prepare the product from the substrate shown N. N. ------->For Step (1) and (2), Draw the Structure OF the product For both of them. OH (1) Ts Cl, PY (2) Na SH,DMSO
- The hydrolysis of tert-butyl chloride proceeds less rapidly in a solvent mixture which is 15% water/85% acetone than in one which is 85% water/15% acetone. Why? O The reaction proceeds by an SN2 mechanism wherein the rate is increased by increasing the concentration of the nucleophile water. The solvent which contains a greater percentage of water is less polar, and this destabilizes the tert-butyl chloride. O None of the above. O The reaction proceeds by an SN1 mechanism wherein the rate is increased by increasing the concentration of the nucleophile water. O The transition state in the carbocation formation step is better stabilized in the more polar solvent mixture.1. Starting with the given substrate and conducting the first reaction step described, provide the COMPLETE CORRECT CONDENSED STRUCTURAL FORMULA for the MAJOR substrate product of the first reaction. 2. THEN, use the major substrate product of reaction step 1 as the substrate of reaction step 2. Conducting the second reaction step described, provide the COMPLETE CORRECT CONDENSED STRUCTURAL FORMULA for the FINAL MAJOR substrate product after reaction step 2 is complete. Remember the reaction rules! It will help to work this problem out on scratch paper with structural drawings.) HERE IS THE DESCRIPTION: Start with the condensed structural formula CH3-C(OH)(CH3)-CH2-CH2-CH2-CH3, and react it first with H2SO4 and high heat, to produce a major substrate product. Then, take that major substrate product, and use it as the substrate of the next reaction, by reacting it with Br2 (in the presence of CH2CI2 solvent), to produce the FINAL MAJOR substrate product. The complete correct condensed…Which statement best describes what is happening in step 6? (Remember, this is copied from the full mechanism, in which we saw the compound on the right being converted into the compound on the left.) CH;-CH,-C-CO, || ΝΗ CH;-CH=Ç-CO, | NH, O reduction O none of these O enamine-imine tautomerization O enol-ketone tautomerization oxidation