2. For the following reaction scheme a. Propose an efficient synthesis for the transformation of 3-methyl-1-butene to 3- methylbutan-2-one. b. Then explain how you could use IR and 'H NMR to distinguish each of the intermediates from each other to track reaction progress. 3-methylbut-1-ene 3-methylbutan-2-one
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- please quickly thanks ! 3.Please write out the major reaction and side-reaction in the preparation of ter-butyl.chloride, and write out the key points to use separation funnel in this process.Conformation control of reaction mechansims. Consider the reaction below: Provide all possible elimination products from this reaction and identify the major elimination product. Provide mechanisms (with curved arrows) that clearly explain the reaction outcome.Fast pls in 5 min will give u like for sure Create a synthesis of the heterocyclic compound 5 from starting materials each containing no more than six carbon atoms.In the solution you should use retrosynthetic analysis to justify your choice.
- Please help me with the a proposed Williamson ether sysnthesisi for 3-ethoxyhexane. Thank you !After the reduction of camphor with NaBH4 experiment, you took a 1H-NMR of your product sample. The sample ave the following 1H-NMR singlas with the given integrations (2.314 and 9.497). Determine the product ratio of isoboreneol to borneol in this particular mixture.i need help with predicting the Ir spec for the final product i also need to make it look like the example with the table and the 1h-nmr digram i made an example of how it needs to look like the lab called Electrophilic Aromatic Substitution: Friedel-CraftsAlkylation
- can i get help drawing out actual structures including the nucleophilic addition of Cy2NH to parafomaldehyde and its hemiaminal intermidiate and the condensation step when it is displaced by terminal alkyne forming allene, also what is dioxane getting rid of as the solvent, thanksAn organic lab student carried out the reaction of methylmagnesium iodide with acetone(CH3COCH3), followed by hydrolysis. During the distillation to isolate the product, she forgot to mark the vials she usedto collect the fractions. She turned in a product of formula C4H10O that boiled at 35 °C. The IR spectrum showed onlya weak O¬H stretch around 3300 cm-1, and the mass spectrum showed a base peak at m>z 59. The NMR spectrumshowed a quartet (J = 7 Hz) of area 2 at d 3.5 and a triplet (J = 7 Hz) of area 3 at d 1.3. Propose a structure for thisproduct, explain how it corresponds to the observed spectra, and suggest how the student isolated this compound.The following IR and NMR were obtained for Alicia’s Intermediate product, Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride. Label all hydrogens with the data from 1H NMR. Label all carbons with the provided data from 13C NMR.
- Explain why the following reaction is not a good way to prepare 1-phenylpentane: benzene + 1-chloropentane + AlCl3 → 1-phenylpentane In your scratch work, give the full, curved-arrow mechanistic explanation of what would happen, and indicate what would likely be your main product or products.The following IR and NMR were obtained for Alicia’s final product, Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid. Label all hydrogens with the data from 1H NMR. Label all carbons with the provided data from 13C NMR.c) FT-IR spectra of both nitro and nitrito-isomers were recorded immediately after preparation. Then small samples were exposed to heat (in oven) and their spectra were recorded again.