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- Predict the major products formed when 2- methyl-1-butene reacts with: H2, Pt/25°C. Show the reaction mechanism the given alkene reactionsM 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :Tunicates are marine animals that are called "sea squirts" because when they are taken out of water, they tend to contract and expel seawater. Lepadiformine is a cytotoxic agent (toxic to cells) isolated from a marine tunicate. During a recent synthesis of lepadiformine, the investigators observed the formation of an interesting by-product (3) while treating diol 1 with a reagent similar in function to PBr3 (J. Org. Chem. 2012, 77, 3390–3400):
- [VII4,5] Instructions: Answer the following: (Refer to the photo below) 4. What is the structure of compound C? 5. What is the structure of compound A?#20 B Draw structural formulas for all possible carbocations formed by the reaction of each alkene with HCl.KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanone
- N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reaction2. How many substitution product/s is/are formed when metabromo anisole is treated with ammonia?A. 0-no reactionB. 1C. 2D. 32. Draw the reaction and resulting product when 1-heptyne is trrated with excess HBr? Draw the reaction and resulting product when 1-ethyne in H20 is treated with H2SO4 + HgSO4?
- 4. Write the complete mechanism of Li/NH3 Reduction of an Alkyne. Show the directions of the electron flow with the proper arrow orientations. Name the final Product. 5- What is order of acidity of the following starting from the least acidic to the most acidic? Alkanes, Alkenes, Alkynes, Aldehydes, Alcohol, Aldehydes, Carboxylic acids. 6- Prepare cis-2-butane using propyne, and alkyl halide. Use any other reagents needed. 7- Use 4-Octene as the only source of carbon in the synthesis of Butanal. Use any inorganic compounds necessary. 8- Draw the structures of: 1-Iodobutane, 2-Iodobutane, 1-Chlorobutane, 2-Bromobutane, and 3-Flouropentane.Chemistry 60. Give the principal product(s) expected, if any, when trans-1,3-pentadiene reacts under the following conditions. Assume one equivalent of each reagent reacts unless noted otherwise. (a) H2O, H3O+ (b) Na+EtO- in EtOH (c) Maleic anhydride heathow did you get the answer for part a: (s)-butan-2-ol , and how did you get the answer for part b