Suppose one is investigating the 1,2 vs 1,4 addition depicted below. What would be an example of an organometallic reagent that would produce the two different products and what is the control feature? H3C H3C Metal ག་ནི་” -CH3 H₂C H3C H3C CH3 OH -VS- H3C- -CH3 H₂C CH 3
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- Question 11 Propose best Williamson ether syntheses for the following compounds. Select all applicable options (multiple answers can be possible). Note: Some compounds cannot be made using Williamson synthesis reaction. A: Хон OH ΚΗ مر OK Br SN2 KH B: OH OK SN1 C: Α ABC ☐ C 1000 Br Cannot be synthesized using Williamson ether syntheses.Question 13 Propose best Williamson ether syntheses for the following compounds. Select all applicable options (multiple answers can be possible). Note: Some compounds cannot be made using Williamson synthesis reaction. ΚΗ A: + ⚫OH ΕΘ OK SN2 KH ΘΘ + -Br B: -OH OK SN1 C: ☐ A B ☐ C Cannot be synthesized using Williamson ether syntheses.(b) The activating and deactivating groups could affect the position(s) of the next incoming group(s) to the benzene ring. Based on the structure below, analyze and explain the group(s) on the benzene ring is activating or deactivating group. Then, identify the product(s) formed from the following reactions. H H;C-C-c CH, Br AIC13 NH, so, H,SO4 (ii) NH, Hfos CH;C1 AICI, (iii)
- Cyclohexene has the formula C6H1o and the structure shown in Figure 4-4. When cyclohexene is treated with acid and water it forms Compound A with the formula C6H12O. When Compound A is treated with an oxidizing agent, it forms Compound B with the formula C6H100. IR spectra for Compounds A and B are shown in Figure 4-3. The best structure for A is The best for B isPropose best Williamson ether syntheses for the following compounds. Select all applicable options (multiple answers can be possible). Note: Some compounds cannot be made using Williamson synthesis reaction. ـيـة A: -OH Na Na Br -Br SN2 Na CI B: -OH C: B ☐ C -CI Na O SN1 Cannot be synthesized using Williamson ether syntheses. MacBook Air 80 000 AA DII F3 F4 F5 F6 F7 F8 DD F9In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a hydride shift accompanied cleavage of the carbon–oxygen bond in the alkyloxonium ion? What ion would be formed as a result of a methyl shift? Which pathway do you think will predominate, a hydride shift or a methyl shift?
- Draw a structural formula for the major organic product of the reaction shown below. + (CH3CH₂)2CuLi • You do not have to consider stereochemistry. √ [F ? ChemDoodleⓇ ether H₂O +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-hydroxyoxiranea) M₂C. Step 4: c) 1H-NMR analysis of product A C D The hydrolysis of an emide involves the cleavage of the amide bond, which is a carbonyl group (C=0) bonded to a nitrogen atom. This reaction is typically catalyzed by an acid or a base. E Step 3: b)IR analysis of product A: The broad peaks in the range of 3500 cm³ to 2500cm* indicate O-H stretching frequency of COOH functional group... The strong, narrow peak around 1720 cm* indicates C=0 stretching frequency of COOH. The medium, sharp peak around 1600cm* indicates C-C stretching frequency of benzene ring Proton A: The small, broad peak around 12 ppm indicates O-H of COOH. Proton B and proton C: The doublets at 8.1ppm, 7.1ppm indicate di-substituted benzene. Proton D: The quartet at 2.4 ppm indicate CH₂ unit with adjacent CH₂ unit. Proton E: Triplet et 1.1 ppm indicate CH₂ unit with adjacent CH₂ unit. Proton label relative integration A 1 B 1 1 2 3 Solution HH₂O Heat H₂G. 1600 cm Product A chemical shift 12ppm 8.1ppm 7.1ppm 24ppm…
- The functional group will have a sharp, dagger-like absorbance at 2220-2250 cm-1 on its IR spectrum (and an odd-numbered molecular mass (M+) on its mass spectrum). O alkyne O nitrile O aldehyde O alkene O carbolxylic acidMIJIUNPICII REJUURUES Copy of Mastery- C11T11Q6758 Preparation and Reactions of Ethers Give the major product(s) of the following reaction. Question 1 Question 2 Question 3 Question 4 Question 5 Question 6 Question 7 Question 8 Question 9 Question 10 ? HBr (1 mole) -OMe heat CH3OH Review Score -OH Review Results by Study Objective obile Site -Br CH3Br There is no reaction under these conditions or the correct product is not listed here.Question 14 Propose best Williamson ether syntheses for the following compounds. Select all applicable options (multiple answers can be possible). Note: Some compounds cannot be made using Williamson synthesis reaction. همه ΚΗ A: LOH ΘΘ OK Br SN2 Br NaH B: ⚫OH -ONa SN2 C: A B C Cannot be synthesized using Williamson ether syntheses.