please be specific, thank you. mechanism that would lead to the Ex. carry out the halogenation...
please be specific, thank you. Ex. draw the major product UV
Please put it in bullet points or numbered. Please and thank you. :) Reaction Mechanism (Draw a stepwise mechanism for the formation of the product 4-methylacetophenone) Reaction Mechanism Discussion (One mechanism discussion for your product) Describe the reaction mechanism using two or less sentences per step of the mechanism. Refer to the introduction section and your organic chemistry textbook to write a well-organized mechanism discussion.
Q: Draw out the mechanism. Please show all steps so I can understand. Thank you! arrow formalism to describe how the reaction below occurs. Be sure to draw out all reaction intermediates & the movement of all electrons needed to justify the formation of the indicated product. You do not need to add in any reagents that are not shown OR show any other products that could be made but are not shown (focus on showing the mechanism for only...
please answer completely and clearly. thank you! SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N SHORT ANSWER #29: How would you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) NH2 N
Write a mechanism for the following radical halogenation reaction. Also, do you happen to know how i would enter this into the online system?? Problem 10.18 Write a mechanism for the following radical halogenation reaction. hv Draw the initiation step of the mechanism. Include a one pairs, formal charges and radicals in the mechanism. Edit
please help! thank you 47) Draw out the reaction mechanism for a Fischer esterification reaction with ethanol and benzoic acid in hot acidic conditions. Name the products. 48) Draw out the reaction mechanism for a Fischer esterification reaction when 5-hydroxyhexanoic acid is heated. Name the products if you feel ambitious.
When cyclopentone was treated with bromine in methanol as solvent, dibromide U and 00-halogenation product V were observed. 62 MeOH ‘OME 7 (a) Explain briefly the formation of anti-dibromide U instead of syn-dibromide in this reaction with the aid of reaction mechanism. (2 marks) (b) Account for the formation of co-halogantion product V in this reaction. (2 marks) (c) Suggest a modification to the reaction condition such that ONLY dibromide U would be formed. (1 marks) (d) Suggest a modification...
please answer clearly and completely. thank you! SHORT ANSWER #30: How would you carry out the synthesis below? Additional carbons may come from any alkyl halide with 3 C's or less. Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms for each step. (10 points) t
Could you please help and answer this question by drawing the mechanism for the reaction and show a possible reaction condition that would allow the product to be the only one forming? If you can explain how and why that would be greatly appreciated. Thank you!! 4. In place of the written protocol show the mechanism of the following reaction and determine how many products can form. Indicate the full mechanism for ONE product formation but show all potential final...
Could you please help and draw this mechanism? Thank you! 3. Ille meeldiSM UI we ledCLIUI. 4. In place of the written protocol show the mechanism of the following reaction and determine how many products can form. Indicate the full mechanism for ONE product formation but show all potential final products that can occur. Reactions must be hand-drawn! KH ethanol