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- 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?for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow mecanism. based on the reaction products, explain why a carbocation intermediate cannot be proposedDraw the curved arrow mechanism for the reaction between (2R,3S)-3,5-dimethylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms. Then answer the question about the mechanism.
- Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productwhy does this carbocation go through rearrangemnt by a hydride shift?Predict the product(s) of this reaction by interpreting the flow of electrons as indicated by the curved arrows.
- Please use curved arrows to show the electron movement, bond making and bond breaking in the concerted reaction below. Thank you!draw the potential products in the space below, for the halogenation (with heat/UW light) reaction:The quick rule which allows prediction of the major product for electrophilicaddition reactions to alkenes (such as shown in question 2) works mechanisticallybecause the electrophile adds to theC=C in the directionthat forms the (a) least stable carbocation, (b) most reactive nucleophile, (c) moststable carbocation,(d) lowest classification of halide.
- In the information provided,-see photo, we read that the axial attack is preferred for the reaction. Explain this preference for the axial attack and the trans product formedin Figure 1. Be sure to comment on the steric factors of the substituents, their placement onthe ring, and the hydride delivery agentDraw curved arrows to represent the flow of electron during the reaction for each of thefollowing reactions.Give a full curved arrow mechanism for the ring-opening reaction of an epoxide in aqueousacid shown below. Show ALL non-bonded electron pairs and all non-zero formal chargeswhere applicable. (Note: you will need to redraw the structures provided in order to showthe mechanism correctly; non-bonded electron pairs have not been shown, although nonzero formal charges are included.) Be sure to show any stereochemical elements in theproduct(s) correctly.