I am having trouble with this reaction. Please show the complete reaction mechanism (with explanantions) for...
Please help me in writing a detailed mechanism for the above reaction. I am having trouble determining if it is an aldol addition. Usually those are with aldehydes as the starting material? Thanks in advance!! O NaOH, H2O b. heat
I need help in Organic Chemistry! I am having trouble with these problems, please help!! I appreciate you! 4. For each of the following sets of material and products propose a synthesis using reactions from Chapters 1-11 of the textbook. Remember to consider stereochemistry where appropriate. Show the product of each step you propose. There are more than one solution for each You do NOT need mechanism, only conditions. a. H-CEC-H
I am having trouble with this question, please show all work so I can understand. Thank you ! 1. Find the means, medians, and SDs of each of the two variables (X and Y) in the chart below. Make sure to show all of your work (15 points; 7.5 points each)
I am having trouble differing between Sn1, Sn2, E1, and E2 reactions. Please help me understand how to approach these problems. I've attempted to answer them, but I am not confident in my answers. Please show me how to get to the correct answer. 1. [is it A?] 2. [Is it C?] 3. [is it 3 and 4?] A) I B) II C) III D) IV E) I and II F) III and IV Predict the mechanism (S\2, E2, SN1,...
I'm still having trouble with the mechanism. Please help. Please predict the product of the following reaction (5). Reaction 5 NaOMе MeOH
Please show complete arrow pushing mechanism for the following reaction. The answer had three products and I am not sure why.
I am having trouble figuring this out. This is for a class called Computing Essentials Complete the timing diagrams below for an edge-triggered D Flip Flop (rising edge implied). Assume the output is 0 initially.
this is an organic chemistry synthesis question, and I am having a little bit of trouble getting started. Any help with the mechanism would be appreciated! thanks! 2. The following reactions are from an article published by Masamune and Sharpless in Science, describing stereoselective synthesis of hexose sugars. a) The following conversion requires two reaction steps, the second one being protection of a diol as a cyclic acetal. Draw a reasonable mechanism for the first step of this reaction (NaOH,...
In organic chemistry, we are learning multistep synthesis but I am having trouble with it. Please help with this problem. OH
This is an E1 reaction, I am having trouble getting the products for it though. Part 1 (2.5 points) Feedback M See Periodic Table See Hint Draw the intermediate formed in the reaction. Part 2 (2.5 points) Feedback See Hint Draw the product(s) formed in the reaction.