Which among the following compounds is best described by the following staterments? Choc NO2 HO. Br GUI SOLO KAO Yields only one major organic product upon nitration: Choose... Yields two isomeric organic products upon treatment with Br/FeBry Choose...
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- Predict the organic products for the reactions indicate major and minor if applicable. Answer all questions pls thanks!Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .tert-Butoxycarbonyl azide was developed as a reagent for peptide synthesis at OWL's home institution, the University of Massachusetts, by Prof. L.A. Carpino. It is prepared by treating tert-butoxycarbonyl chloride with sodium azide. Propose a structure for the initially-formed intermediate in this reaction.
- provide the products and stereochemistryInterestingly, reduction of the complex shown above mostly gives thealcohol enantiomer shown below after workup. a. Draw the other minor diastereomeric alcohol product. b. Briefly explain the diastereoselectivity of the reduction – why is oneenantiomer heavily favored? Draw a structure or structures to support youranswer.Although diazomethane (CH2N2) is often not a useful reagent forpreparing cyclopropanes, other diazo compounds give good yields ofmore complex cyclopropanes. Draw a stepwise mechanism for theconversion of diazo compound A to B, an intermediate in the synthesisof sirenin, the sperm attractant produced by the female gametes of thewater mold Allomyces.
- 4.4 Show how the compound thiodiazine - C21H26N2S2 - decomposes anaerobically and how these end products in turn decompose aerobically to stabilized sulfurand nitrogen compounds.One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.provide the major profucts ( wrote "no reaxtion "if you think so) for the following reactions with correct stereochemistry. Please explain step by step with explanation
- 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?What is /are organic product(s) expected when 1-butyne is first treated with sodium amide and the resulting acetylide anion reacts with tert-butyl chloride before aqueous acid workup?An inexperienced graduate student treated dec-5-ene with borane in THF, placed the flask in a refrigerator, and left for aparty. When he returned from the party, he discovered that the refrigerator was broken and that it had gotten quite warminside. Although all the THF had evaporated from the flask, he treated the residue with basic hydrogen peroxide. Tohis surprise, he recovered a fair yield of decan-1-ol. Use a mechanism to show how this reaction might have occurred.(Hint: The addition of BH3 is reversible.)