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- c) rite in the reagent(s) over the arrow. a) C6H5N₂+ b) C6H5C=N H3C- An OH H₂C → benzene H3C benzylamine CI CH3Use the dropdown menus to choose the correct name for each structure shown. V [ Select ] H. 2-methylbenzoic acid CH3 ethylcyclocarboxylic acid 2-methylcyclocarboxylic acid 2-ethylbenzoic acid ( Select ) -C-OH O CH, -CH,-C [ Select] CH, | Select ) CH,-CH-CH2-c-o-CH, CH-CH-NH-CH, CH, | Select ) H3C CH3 'N | elect ] Use the dropdown menus to choose the correct name for each structure shown, ( Select ) H. CH3 COH V[ Select ) 2,2,2-trichloroethanoicacid 1,1,1 trichloro-2-carboxyethane 1, 2,2 chloroethanoic acid 2,2,2-chloroethanoic acid O CH, но---сн,-сн,--он [Select CH, ( Select ] CH-CH, -CH2-č-o-CH, CH,-CH-NH-CH, [ Select ] CH, H3C CH3 [ Select [ Select) H. CH3 [ Select) -c-OH CH, HO-E-C-CH,-CH, CH, OH [Select ) 2,2 dimethyl-1,5-pentanedioic acid 3,3-dimethylpentanedioic acid 2,2-dimethylpetanoic acid CH,-CH, -CH2-c-o-CH 2,2-dimethylpetanedioic acid CH,-CH-NH-CH, CH, ( Select] H3C CH3 'N' [ Select )Give detailed Solution with explanation needed
- Which of the following best describes phenol? Group of answer choices a benzene ring with an OH attached a cyclohexane with an OH attached a cyclohexene with OH attached all of the above are equally good descriptions18:44 1 Reset Question 4 of 12 CI Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 5Gº CI Submit 2- 1,2-3,4- 1,1- 2,2- 1- tert- di tri cyclo sec- iso meth carbo) prop bromo) chloroeth ane yl ene yne Tap here or pull up for additional resourcesGive typed solution with explanation.
- 8) Which compound is aromatic EX b) راه FORa) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.18:45 1 Question 5 of 12 Reset 5Gº Submit Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 3- 2,3- 2,4- 4- 3,4- 2- iso di sec- tri) cyclo tert- hex hept) oct) [meth) pent] (eth yl yne ene ane Tap here or pull up for additional resources
- Synthesize each compound from cyclohexanol using any other organic or inorganic compounds. CH,OH a. g. (Each cyclohexane ring must come from cyclohexanol.) COOH b. d. h. сно CHs (Each cyclohexane ring must come from cyclohexanol.)Choose the most appropriate systematic (IUPAC) name from the choices below that accurately describes the following structure (drawn in a Newman projection). H H. CH3 H;C 3-methyl-4-flouro-1-pentene 4-fluoro-3-methyl-1-pentene 3-methyl-1-alkenyl-4-fluoride 2-fluoro-3-methyl-4-pentene O 4-fluoro-2,3-dimethyl-1-buteneParts D&E Please.