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- dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.When (CH3CH2)3CBr is added to CH3OH at room temperature, the product is (CH3O)C(CH2CH3)3. Propose a mechanism(s) for the reactions leading to these products and used curved arrows to show the movement of electrons.When (CH3CH2)3CBr is added to CH3OH at room temperature, the product is(CH3O)C(CH2CH3)3. Propose a mechanism(s) for the reactions leading to theseproducts and use curved arrows to show the movement of electrons.
- name the major product for the reaction of 4-methyl-1-pentyne with the following reagents ⦁ H2/Li or Na/NH3 (liq) at -78 degrees CThank you for the answer, would it be possible to follow the path I have attached as well srarting from methanol ---> CH3Br -----> CH3MgBr-------> (H3C)CH-CH2OH ----> E1 IsobutaleneDraw the structure of the product that is formed whent he compound 3-hydroxycyclohexanone undergoes a reaction with 1 equivalent of CH3MgI and then is treated with water. So normally the CH3 would attach and break the double bond with the O but this isn't the correct answer.
- For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne (b) hex-2-yne(c) hex-3-yneVShow how you would convert 2-methylcyclopentanol to the following products. Any of these products may be used as thereactant in any subsequent part of this problem.(a) 1-methylcyclopenteneredraw the following reaction mechanism with benzene instead of isoborneol. it's an oxidation mechanism from OH to ketone. please include the arrow pushing.
- what is the expected product S for the following mono alkylation reaction of 2 methyl 4 tert butylcyclohexane under the conditions shown o ch3 lda *not all answer options showncpredict the product of the following reactions of aldehyde and ketoneA hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.