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- Complete and predict the regioselectivity of the following pericyclic reaction: Explain your answer using FMO principlesThe structures of two tertiary bicyclic chlorides (compounds 1 and 2) are shown below. Which of the following statements is correct?Give the major organic product(s) of the reaction shown below. Be sure to show all stereoisomers formed, and indicate which isomers are formed in equal and unequal quantities.
- A 1-butene reacts with can yield butan-1,2-diol when it reacts with potassium permanganate in a basic medium. True or FalseI am working on a practice assignment for my organic II course and am having difficulty with a question that asks to identify the reaction sequence used to synthesize isopropylcyclopentane. I would really appreciate the help!] The reaction of 2-bromopropane and sodium ethoxide in ethanol reacts 6.7 times faster than 2-bromo-1-deuteriopropane under the same conditions. Explain what mechanism this data is consistent with, and why
- When 1,1,3,3-tetramethylcyclobutane is brominated at 125°C, the relative reactivity of the 1°: 2°: 3° hydrogens is approximately 1:82:1600. Estimate the amount of each monobromination product.Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?Can you assist with predicting the organic product(s) of the last two reactions and provide stereochemistry, if applicable.
- please explain and discuss thoroughly the method of isolating betacarotenePredict products of the McLafferty rearrangement for the molecule . Provide high quality drawings and explanations.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, thanks
