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- Describe stereoselective, regioselective, or chemoselective, the reactions below.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.Arrange the following reactions in order of increasing ΔrxnS and briefly explain your reasoning. a) S(s)+O2(g)⟶SO2(g) b) H2(g)+O2(g)⟶H2O2(ℓ) c) CO(g)+3H2(g)⟶CH4(g)+H2O(ℓ) d) C(s)+H2O(g)⟶CO(g)+H2(g)
- Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the helpArrange the following reactions in order of increasing ΔrxnS and briefly explain your reasoning.a) S(s) + O2(g) ⟶ SO2(g)b) H2(g) + O2(g) ⟶ H2O2(ℓ)c) CO(g) + 3 H2(g) ⟶ CH4(g) + H2O(ℓ)d) C(s) + H2O(g) ⟶ CO(g) + H2(g)Arrange the following reactions in order of increasing ΔrxnS and briefly explain your reasoning. a) S(s) + O2(g) ⟶ SO2(g)b) H2(g) + O2(g) ⟶ H2O2(ℓ)c) CO(g) + 3 H2(g) ⟶ CH4(g) + H2O(ℓ)d) C(s) + H2O(g) ⟶ CO(g) + H2(g)
- Propose a plausible mechanism for the 1 to 2 conversion as shown, and explain the stereochemical result:predict the main product for the addition of 1 equivalent of HX to the following compounds and write the mechanism of the reactionPropose mechanisms compatible with 1) and 2) of the following reactions.
- Considering the following reaction, while kinetic resolutions limit your yield of, for example, acetate 3 to 50%, in certain cases this can be improved by using a sequence of reactions that convert the undesired enantiomer to the desired one. Propose a series of such reactions that would allow you to convert the (S)-2 to acetate 3. Thank you :)The E1 mechanism (unimolecular elimination) of Elimination ?The diasteromers of 4-t-butylcyclohexanol that you make can be distinguished by the splitting patterns of the proton attached to the carbon bearing th OH group. This is due to the fact that the H that is axial is a triplet of triplets because it is coupled to to sets of non-eqivalent protons, while the equatorial H is coupled to 4 equivalent hydrogens and is a pentet. True? False? Please answer very soon will give rating surely Complete explaination needed