Specify the reagent(s) suitable for converting 2-methyl-2-butene to 2-bromo-3-methylbutane. Check all that apply. H₂ HBr Peroxides BH3 NaBr Br₂ Peroxyacetic acid None of the above × 5
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- I was trying to synthesize this end product from benzene. I am not sure if the steps after the PoCl3 and pyridine are correct because I know PoCl3 and pyridine give a product that follows Zaitsev's rule. If this is incorrect can you show me the correct way?Specify the reagent(s) suitable for converting 3-ethyl-4-methyl-2-pentene to 2-bromo-3-ethyl-4-methylpentane. Check all that apply. NaBr ☑ ⑤ Peroxyacetic acid Br₂ HBr BH3 Peroxides H₂ None of the aboveThis question has multiple parts. Work all the parts to get the most points. Diazotization of aniline first involves the formation of NO* (nitrosonium ion) by the dehydration of nitrous acid with sulfuric acid. The aniline nitrogen then acts as a nucleophile and eventually loses water. NH2 N2* HSO4 HNO2 H2SO4 a Draw curved arrows to show electron reorganization in this mechanism step. Arrow-pushing Instructions Ph H.
- Can i get help please17 eBook Print References Specify reagents suitable for converting 3-ethyl-2-pentene to 2,3-epoxy-3-ethylpentane. Select the single best answer. peroxyacetic acid 1. B₂H6; 2. H₂O2, HO™ 3 attempts left Check my work O H₂O, H₂SO4 Cr₂0₂², H 03, CH3OHWhen 2-bromo-2-methylbutane is treated with a base, a mixture of 2-methyl-2-butene and 2-methyl-1- butene is produced. When potassium hydroxide is the base, 2-methyl-1-butene accounts for 45% of the product mixture. However, when potassium tert-butoxide is the base, 2-methyl-1-butene accounts for 70% of the product mixture. What percent of 2-methyl-1-butene would be in the mixture if potassium propoxide were the base? base Br A. Less than 45% B. C. 45% Between 45% and 70% D. More than 70%
- $ [References] H₂O + CO₂ + Nal CH₂ HỌC CHO a = Proton transfer d E1 Elimination - f SN1 Nucleophilic substitution = b = Lewis acid/base e E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next> Save and Exit Cengage Learning Cengage Technical Support PrtScn F6 F7 1. 2. O F4 % 5 T OH you. ♫ F5 ^ 6 Y H 1₂ H₂O NaHCO3 & 7 [Review Topics] into * 8 CH₂ H₂CH₂ CH₂ I F8 K + 73°F Sunny Home 9 O F9 L ) End 0 8:14 AM □ 6/20/2022 PgDn E = P P B F10 PgUp 4x F11 F12 InsChoose reagents to convert 2-cyclohexenone to the following compounds.Question 8 Select an acceptable name for the compound below. (Stereochemistry is not indicated.) OH 2-(3-butenyl)-1,2-epoxy-1-ethanol 2-(3-butenyl)-3-hydroxyoxirane 5,6-ероху-6-hydrоху-1-hexene 3-(3-butenyl)-2-hydroxyoxirane
- iii) 2-Bromo-2-cyclopropylpropane will undergo an SN1 reaction called solvolysis in methanol to give several products, two of which are shown below. Use curly arrows to show how the formation of these two products occurs mechanistically.Part I (Quantitative): a substitution reaction using the tertiary diol below will produce a product that can be isolated and characterized. на хот 2,5-dimethylhexane-2,5-diol conc. HCI The available reaction solutions are: ▪ 18% sodium iodide in acetone ▪ 1% silver nitrate in ethanol 2,5-dichloro-2,5-dimethylhexane m.p. 63-66.5 °C Part II (Qualitative): the substitution of various alkyl halides will provide insight into the effects of substrate structure, leaving group, and reaction temperature on SN2 and SNl reactions, and you will be able to draw conclusions about these reactions based on your observations. The available alkyl halides are listed later in the experimental procedures section. For Part I (Quantitative): a. Draw the overall synthetic reaction, including all structures, relevant physical data, amounts, and safety information. b. Clearly show the calculation (including units throughout) of the theoretical yield of the reaction. Indicate the limiting reagent. For Part II…16 eBook Print References 3 attempts left Check my work Specify reagents suitable for converting 3-ethyl-2-pentene to 3-ethyl-3-pentanol. Select the single best answer. O H₂, Pt HCI H₂O, H₂SO4 peroxyacetic acid 1. B₂H6; 2. H₂O₂, HO™