12.2. Predict the products of the following reactions. Be careful to consider all stereochemical aspects. CH3 CH3 m-chloroperoxy- benzoic acid (b) H2C (g) H CH2 OsO4 H. (k) OH t-BUOOH VO(acac)2 CH3
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- Can you assist with predicting the organic product(s) of the last two reactions and provide stereochemistry, if applicable.I 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!Hydrocarbon 10 and ester 12 react upon heating to give a cycloaddition product D. (i) Suggest a structure for product D and provide a curved arrow mechanism that accounts for its formation. (ii) Draw the molecular orbitals corresponding to the HOMO of 10 and the LUMO of 12 and show that these are of suitable symmetry for a concerted cycloaddition to take place. (iii) Use frontier molecular orbital theory to account for the observation that the formation of D is faster in the presence of AlCl3. please answer all thank you
- Grignard reagents react with oxirane (ethylene oxide) to form 1° alcohols but can be prepared in tetrahydrofuran solvent. Why is this difference in behavior observed? A. There is a better leaving group in the oxirane molecule. B. Steric hindrance in the case of tetrahydrofuran precludes reaction with the Grignard. C. It is easier to obtain tetrahydrofuran in anhydrous condition. D. Oxirane is a cyclic ether, while tetrahydrofuran is a hydrocarbon. E. The oxirane ring is the more highly strained.1. Give the major organic product(s) of the reaction and include all the stereochemistry as appropriate. Identify any meso compounds. 2. Indicate whether a solution of the product would be optically active or no not active and provide a simple reasoning to support your choice.Nitrating methyl benzoate. 1.Describe the mechanism of EAS clearly and in detail 2. What is the effect of subtituent of the outcome of EAS；include 3 classes of subtituents
- 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?For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Over the past several decades, chemists have developed a number of synthetic methodologies for the synthesis of steroid hormones. One of these, developed by Lutz Tietze at the Institut für Organische Chemie der Georg-August-Universität, Göttingen, Germany, used a double Heck reaction to create ring B of the steroid nucleus. As shown in the following retrosynthetic analysis, a key intermediate in his synthesis is compound (1). Two Heck reaction disconnects of this intermediate give compounds (2) and (3). Compound (2) contains the aromatic ring that becomes ring A of estrone. Compound (3) contains the fused five- and six-membered rings that become rings C and D of estrone. Q.Propose structural formulas for compounds (2) and (3).
- Over the past several decades, chemists have developed a number of synthetic methodologies for the synthesis of steroid hormones. One of these, developed by Lutz Tietze at the Institut für Organische Chemie der Georg-August-Universität, Göttingen, Germany, used a double Heck reaction to create ring B of the steroid nucleus. As shown in the following retrosynthetic analysis, a key intermediate in his synthesis is compound (1). Two Heck reaction disconnects of this intermediate give compounds (2) and (3). Compound (2) contains the aromatic ring that becomes ring A of estrone. Compound (3) contains the fused five- and six-membered rings that become rings C and D of estrone. Q.Name the types of functional groups in estroneOver the past several decades, chemists have developed a number of synthetic methodologies for the synthesis of steroid hormones. One of these, developed by Lutz Tietze at the Institut für Organische Chemie der Georg-August-Universität, Göttingen, Germany, used a double Heck reaction to create ring B of the steroid nucleus. As shown in the following retrosynthetic analysis, a key intermediate in his synthesis is compound (1). Two Heck reaction disconnects of this intermediate give compounds (2) and (3). Compound (2) contains the aromatic ring that becomes ring A of estrone. Compound (3) contains the fused five- and six-membered rings that become rings C and D of estrone. Q.How many chiral centers are present in estrone?Over the past several decades, chemists have developed a number of synthetic methodologies for the synthesis of steroid hormones. One of these, developed by Lutz Tietze at the Institut für Organische Chemie der Georg-August-Universität, Göttingen, Germany, used a double Heck reaction to create ring B of the steroid nucleus. As shown in the following retrosynthetic analysis, a key intermediate in his synthesis is compound (1). Two Heck reaction disconnects of this intermediate give compounds (2) and (3). Compound (2) contains the aromatic ring that becomes ring A of estrone. Compound (3) contains the fused five- and six-membered rings that become rings C and D of estrone. Q.Show how your proposals for compounds (2) and (3) can be converted to compound (1). (Note: In the course of developing this synthesis, Tietze discovered that vinylic bromides and iodides are more reactive in Heck reactions than are aryl bromides and iodides.)
