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- Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Draw the structure of the major organic product(s) of the reaction. You do not have to consider stereochemistry. 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.Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after workup to neutralize acid. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
- Carbocations rearrange with some ease. An example of this is shown below. Indicate, with the corresponding arrows, how this process occurs. The carbocation 2 is more stable than 1, why is this? Explain it using (drawing) structures.The question is: "Draw the curved arrow mechanism for the reaction between (2S,3S)-3-methylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms" I attached screenshots of the picture of the atoms below. What type of reaction (SN1, E1, SN2, or E2) would the reaction be, and how would these molecules interact? The question asks for multiple steps so I am guessing it is either SN1 or E1, but what is the reaction mechanism?Draw the structure of the major organic product(s) of the reaction. You do not have to consider stereochemistry. All carboxyl and amino groups should be drawn in the neutral form. If no reaction occurs, draw the organic starting material. 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.
- please point out the ones that are the resonance structure of the most stable carbocation, please.draw an energy diagram that follows the criteria belowPredict the product or starting material of the following alkene addition reactions. Remember, Hydride shifts are possible if/when a more stable carbocation can exist! Put your answers (organic products only) in the indicated boxes.
- This question has multiple parts. Work all the parts to get the most points. a Draw all of the monochlorination products that you might obtain from the free-radical chlorination of 2,2,4-trimethylpentane. You do not have to consider stereochemistry. 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.Predict the products of this organic reaction: Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area.Please help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.