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- Which of the following molecules is most nucleophilic? OA. NaOCH₂CH3 OB. CH3CH₂OH OC. NaOC6H5 OD. C₂H5OH 1 E.CH3COONaSelect the reagent(s) necessary for the given step of these synthesis pathways: Reagents available a. CH3 CH2 COCi f. PB33 b. C6 H5 COCI g. Mg, ether c. AlCl3 h. H2SO4, conc d. NaBH4, ethanol i. SOCI2 e. Н,SO4, dil j. C6H5 CN Scheme 1: он Br CH3 CHa CH3 MgBr CH3 C-H CH,CH3 но CH2CH3 Step 2 : Previous Next Step 7:Use the reaction given below to answer the following questions. A CH₂OH B H₂O+ C + CH3NH3* D a) What are the approximate pKas of compounds A and B? b) The reaction given above is irreversible. Give a detailed explanation of the reaction and reaction mechanism. Your explanation should indicate your knowledge of the reactivity of carboxylic acid derivatives.
- Which one of the following synthetic routes gives the best yield of meta-bromoaniline starting with benzene? NH2 HNO, 1) Sn. HCI Br, A. FeBr, H,SO, 2) NaOH Br metabromoaniline 1) Sn, HCI Br, HNO, В. H,SO, 2) NaOH FeBr, HNO, Br, 1) Sn, HCI C. FeBr H,SO, 2) NaOH 1) Sn, HCI HNO Br, D. 2) NaOH HSO FeBr, O A O B O C Ouestion 14 6 pts MacBook Pro Search or type URLArrange the following compounds in INCREASING reactivity towards Nucleophilic Acyl Substitution. ABC O Jh Br O DEF INCREASING REACTIVITY: choose your answer... NH₂ GHI choose your answer... OH < choose your answer...How many elimination products will be formed in the following reaction?
- Identify all reactions supported by the substrate below. O a. Sn1 O b.SN2 O C. E1 O d. E2 O e. SN1 & E1 f. SN2 & E2 O8 SN1, SN2 & E1 O h. SN1, E1 & E2 i. SN2, E2 & E1 O j. SN1, SN2, E1 & E22. Given the following sequence of reactions, draw the structure of products A and B and write a detailed reaction mechanism that explains their formation. H2N H30* A B 3. Write a detailed reaction mechanism for the following transformation. Upload your answer as an attachment. OEt OEt OEHelp me
- Propose a synthetic pathway for the conversion of each of the indicated starting materials into the respective products EtzN. HO. HO. `CO2E1Select the reagent(s) necessary for the given step of these synthesis pathways: Reagents available a. f. PBr3 CH3CH2COCI b. C6H5 COCI c. AlCl3 g. Mg, ether h. H2SO4, conc d. NaBH4, ethanol i. SOCI₂ e. H2SO4, dil j. C6H5 CN Scheme 1: Step 7: Step 2: Scheme 2: MgBr CH3 H3C CH3 H3C Step 5: Step 3: CH3 2 OH OH CH3 3 HO-C-C-H Br CH3 CH2CH3 CH2CH3 MgCl 3 2 H3C CH3 CH3 H3C CH3 5 6 .OH H3C CH3 H₂C CH₂ H3C CH3Identify the best reagents to complete the following reaction. 1. NaOH A 2. CH3CH2CH2NH2 1. HCI В 2. CH3CH2CH2NH2 ОН CH3CH2CH2NH2 C 1. SOCI2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCI2 NH,