Draw the major organic product of the reaction shown below. OH K₂Cr₂O7 H₂SO4, H₂O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.
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- 1 example of reaction for each of the types of organic reactions: substitution, elimination, addition, and rearrangement. Show:a. the overall reaction (reactants --> products)b. the reaction mechanism (indicate intermediate product)c. indicate which is the reactive species or intermediate in the reaction (radical? electrophile? nucleophile?)d. overall description of the reaction eg., radical substitution or SRGive all possible monosubstituted products for the reaction between propane and bromine in the presence of light. Determine the major product. I know the major product is 2-bromopopane but can I want to know if what im doing is right :) I used relative yieldThe substitution reaction below forms two ehters (which are consitutional isomers). Please draw the structures of the 2 ethers formed. Are the ethers single enantiomers or racemic mixtures?
- In the reactions given below, write to which organic molecule Y, Z, T, A ‘belongs, and give information about the reaction types that take place.Show full curly arrow mechanims and please talk about regioselctivity/stereoselctivity. Also, define which one is nucleophile, electrophile, base/acid/reducing agent and reaction name. Please draw a new one. Thank youFill in what the structures in the boxes should be. This appears to be SN1 to get to the first box, E2 to get to the second, and electrophilic addition to get the final product. Assuming that that's correct, yes it's great I got that, but I'd like to confirm how the whole thing should look.
- Please explain the reaction mechanism above to show how product is formed. The product is the borate coplymer .( Please include ALL lone pairs with the structures and provide an explanation of what is happening)please solve this step by step with clear explainationShow full curly arrow mechanims and talk about regioselctivity/stereoselctivity. Also, define which one is nucleophile, electrophile, base/acid/reducing agent and reaction name. Thank you
- I have attached the reaction and mechanism. So please discuss any stereochemistry issues or regioselectivity. Is there any selectivity? Or by using PPh2 there is some selectivity?? I don't understand how much simpler I can make this question as it keeps getting rejected by experts.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.What is the main organic product (B) of the reaction scheme in Figure 11?