6) Design efficient synthesis. Write the reagents needed for each step and intermediate products.(1 i) CH3CH₂CH=CH₂ ii) CH3CH₂CH=CH₂ i CH3CH₂CH₂COH (4 C atoms) CH3CH₂CH₂CH₂COH (5 C atoms)
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- Finished A-C need help with the remaining D-IIdentify the reagents needed to come up with the given compounds. Pls Separate the reagents with a comma and a space. (ex. HNO3, H2SO4). For a multi-step reaction, separate the reagents with a semi-colon. (ex. HNO3, H2SO4; CH3Cl, AlCl3) There should be 9 reagentsWhich compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaF
- For the nitration of a monosubstituted benzene, which substituent, when attached to benzene, produces the fastest reaction rate? —Br —CH3 -OCOCH3 —OCH3Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.which c-h bond has the lowest BDE (bond disassociation energy)?
- Please help with this ochem mechanism... 1. Provide the stepwise mechanisms of the given reaction a) o,p-dinitrochlorobenzene + NaOHIn some nucleophilic substitutions under SN1 conditions, complete racemization does not occur and a small excess of one enantiomer is present. For example, treatment of optically pure 1-bromo-1-phenylpropane with water forms 1-phenylpropan-1-ol. (a) Calculate how much of each enantiomer is present using the given optical rotation data. (b) Which product predominates—the product of inversion or the product of retention of configuration? (c) Suggest an explanation for this phenomenon.Reagents 1 and 2
- ONLY USE THINGS LEARNED IN ORGANIC CHEM 1 Show stepwise mechanism by pushing arrows (Fishhook) and drawing all intermediates: Draw a detailed mechanism for the addition of HBr to 3,3-dimethyl-1-butene in the presence of dimethylperoxide. Show and label all steps including initiation, propagation and termination.Identify the correct ranking of the following molecules from most prone to nucleophilic attack at a sp^2 carbon to least. The correct answer is D, but please explain.Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangement