Consider this organic reaction: ox- Draw the major products of the reaction in the drawing area below. If there won't be any major products, because this reaction won't happen at a significant rate, check the box under the drawing area instead.
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- Predict the major products of this organic reaction. Draw only the major product or products in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If there will be no products because there will be no significant reaction, just check the box under the drawing area and leave it blank. Note for advanced students: you can ignore any products of repeated addition.Please help with both parts, as I will be using them to study, reaction A should have 2 products and reaction b should have 3Consider reactions ‘a’ and ‘b’ shown below, then determine which of A to E is true.
- 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.For each of the reactions below, rewrite the mechanistic step, correcting any errors, or state that the step is fundamentally flawed, or state that the step is correct. Do NOT just look at the step, but consider other possibilities that might happen. Keep in mind that mechanisms always happen in baby steps, one simple change at a time.Can you please draw me a specific complete mechanism (as possible) of step 1 and 2 (and circle the part of the mechanism that would be compound 1 and 2 so I can track the work)? start from the reactant, with electron pushing arrows by including all the intermediates and the formal charges.
- Given the reactant Br−Br, add curved arrows to show homolytic bond cleavage, then draw the expected product. Be sure to add any charges and nonbonding electrons that result from the cleavage.You react an unknown aldehyde (substitutent group marked with an "x") with a ketone and get the product on the right (substitutent group still unknown). HNMR data for the product is shown below. Which of these 3 aldehydes is the reactant that was used? sorry the HNMR looks rough, this was the last question on my final and I am still kinda reeling from it.What would the mechanism look like for the reaction below?