For each subsection, arrange the substituents in progressive order of priority based on the OCahn-Ingold-Prelog nomenclature. а) -ОН -OCH3 - COOH -CHO
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- Rank the following groups in order of priority from highest (1) to lowest (3). < < -COO- -CH3 -NHCH3Give the IUPAC name for each of the following: || CH,CH,-0-C-CH,CH, a. b. CH,CH,CH, СН,— С-О-CH,CH,CH,0 || CH,-O-C-(CH2)2 – CH3 O || CH-O - C - (CH2), – (CH = CH – CH2)2 – (CH2)3 – CH3 O || CH,- O-C-(CH2)8 – CH3 - 3 KOH
- The reaction of CH -CH = CH - CH with HOH would form CH3 3. a) CH3 - CH CH - CH3 b) CH3 – C = C - CH3 с) О ОН Н ОН ОН // CНЗ-С-СНЗ d) CH3 - СH2-О-СНGive the IUPAC name for each compound. Part 1 of 3 CH₂CH, H,C-C-CH_CH, CH, 1 H Part 2 of 3 X CH, H H,CCH,CH,-с-с-сH CH CH,CH, I H CH₂CH₂CH, Part 3 of 3 X H CH₂CH₂CH, H,CCH, -e-c-CH,CH, H,CCH, ЙОН а) КН, 18C6 -CH,CH=CH2 CH3 80 °C
- Provide an appropriate name for the following compound. 3-fluro u-methyl 5-chloro 7 OH CI F 5-chbro-3 fluro-4 methyl non-2-enol 2) Draw the molecule that corresponds to (3R,5R,6R)-5-cyclopropyl-6-ethyl-3-iodo-1-methylcyclohex-1-ene.Draw all of the products, both constitutional isomers and stereoisomers, of the following reactions. a) 4,4-dibromo-1-ethylcyclopentene ---->Br2,H2O b) 3,3-dibromo-1-ethylcyclopentene ----> HBr c) 3,3-dibromo-1,2-dimethylcyclopentene ----> 1. BH3. 2. H2O2, NaOH= highest priority group, 4 = lowest Rank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 priority group). -CH2BR -H -OH -CH3
- C\ Rearrangement the following structures by increasing melting point? CH3 CH3 ÓH D\ Rearrangement the following structures by increasing boiling point? СООН CH3 NO2Explain the different products of the following two reactions by considering the mechanism by which each reaction proceeds. As part of your explanation, use the curved arrow formalism to draw a mechanism for each reaction. CH,OH CH2=CH-CH-CH, + Na*¯OCH, CH;=CH-CH-CH3 Br OCH, CH,=CH-CH-CH, + CH,OH – CH,=CH–CH–CH, + CH,CH=CHCH, Br OCH, OCH,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-