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- Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank you1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]Provide structures of the reactant/products: 1. MgBr 1. KCN a) 2. Нзо" 2. H30* 1. CH;ONa 1. NABH4 2. H30* 2. H30* 6) COOt Na OEt .cOOEt H20* 1. NaOCH2CH3 2. Нао
- PPh3, DIAD CH20H (A) THF mitsunobu H2N sreaction NH2 excess AGOH () (Ci3H20 INS) me I N-me meThe following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.Provide a stepwise synthesis of 1-cyclopentylethanamine using the Gabriel synthesis. NH NK NH HO. OH NH2 Кон; ;H3O+ KOH; ;H30* "Br LIAIH4; ; H3O* Br LIAIH4;
- 6. What are the line structures of compounds E and F in the following sequence of reactions? 0 Compound E L NINH,NH, 2. CH₂CH₂Br Compound F H₂O, H₂SO₂ HgSO; CH₂CH₂CCH₂CH₂CH₂ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamined. e. (Z) (H3C)2N. OCH3 CN
- Select the appropriate synthetic route to convert methylcyclobutane into cyclopentene. ?? 1 1. KOtBu; 2. BH3-THF; 3. H₂O2, NaOH; 4: H₂SO4, heat 1. H₂, Lindlar's catalyst; 2. BH3-THF; 3. H₂O2, NaOH 1. Br₂, hv; 2. KOtBu; 3. BH3-THF; 4. H₂O2, NaOH; 5: H₂SO4, heat 1.BH3-THF; 2. H₂O2, NaOH; 3. H₂, Pt 1. Br₂, hv; 2. KOtBu; 3. H₂O₂, NaOH; 4: H₂SO4, heatCompound A has the formula C5H10O that is produced by oxidation of a conpound that has the formula C5H12O. Compound A has an IT spectrum the has an absorbance at 1700 cm^-1 and no broad absorbance from 2500-3500 cm^-1. The 1H and 13C spectrums of Compound A both have 4 peaks. What is tbe structure of Compound A? Thank you for the help!When naming disubstituted benzenes, incorporate common names, if possible. Designate the positions of the groups relative to each other by numbering the groups, or by using the designations of ortho, meta, or para Trisubstituted benzenes are named by incorporating common names, if possible. If a common name is used, that group is automatically given the designation of #1. Give the lowest numbering possible. Name each of the following compounds: