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- R'R°CHOH-CR'R* R'R?C=CR*R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?ua U LIIUUSE une correct name tor each structure shown. [ Select) H. CH3 [ Select ] a- OH O CH) HO-E-E- -CH,-CH, CH, [ Select ) V [ Select ] CH-CH,-CH2-C-o-CH, methyl butanoate methyl carboxybutane butyl methanoate CH,-CH-NH-CH, CH, methyl butyl ester H3CN-CH3 'N' [ Select ) [ Select ) H. CH3 -OH [ Select ] CI O CH, HO-C -CH,-CH, [ Select ) ČH, ( Select ) CH,-CH, -CH2-č-o-CH, CH,-CH-NH-CH, V[ Select ] CH, 1,1-dimethylbenzne dimethyl-nitro-benzene H3C CH3 N. 1,1 dimethylcyclohexane N-methyl-2-propanamine [ Sel [ Select ] CH3-CH2-CH2-c-o-CH, CH3-CH-NH-CH; ( Select ] ČH3 H3C., -CH V [ Select ] dimethyl-nitro-benzene 1,1 dimethylcyclohexane N,N - dimethylaniline 1,1-dimethylbenzne NH, [ Select) H,C. NH, [ Select ] CH3-CH2-C-NH - CH,Provide the missing reactants and reagents. a is bis c is d is e is 11 V < Previous C 0 NHCH3 (R.S)-Methamphetamine
- R'R?CHOH-CR°R* R'R?C=CR®R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?OH conc H3PO4 A A MCPBA CH₂Cl₂ B NaOH H₂O 8. Identify the products A,B and C.FUNCTIONAL GROUP SUBSTITUENT NAME -X (F, CI, Br, I) halo- -OH hydroxy- -SH mercapto- -OR alkoxy- -NH2 amino- -CHO formyl or alkanoyl -C=0 Oxo-or keto- -COOH carboxy- Alkoxycarbonyl Halocarbonyl -COOR -COX -CN cyano- -CONH2 carbamoyl-
- What is the major organic product of the following reaction? OI || ||| OIV OV 1. LIAH, 2. H₂0 H₂N 101Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.15-41 Compound A(C5Hh, is not optically active and cannot be separated into enantiomers. It reacts with bromine in carbon tetrachloride to discharge the purple color of bromine and form Compound B( C.FL Br,). When Compound A is treated with H., in the presence of a transition metal catalyst, it is converted to compound C(C5H10). When treated with HC1, compound A is converted to compound DtC.HyCl). Given this information, propose structural formulas for compounds A B, C, and D. Hint: There are at least three possibilities for Compound A and, in turn, three possibilities for Compounds B. C, and D.
- Each H↔H eclipsing interaction in ethane costs about 4.0 kJ/mol. How many such interactions are percent in cyclopropane? What fraction of the overall 115 kJ/mol (27.5 kcal/mol) strain energy of cyclopropane is due to torsional strain.90 % ΗΝΟ Product I HO or Product II 70 % HΝΟ;Drawthe MAJOR product(s) of the followingreaction. 1) Hg(OAc)2, H2O 2) NABH4 3) Na,Cr207, H2S04, H2O 1. он 1) NaH 2) 8 3) H2O 2. Fuming H,SO4 3. CH;COCI pyridine 4.