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- Rank the following groups in order of decreasing priority. −F, −NH2, −CH3, −OHRank the following groups in order of decreasing priority. a. – COOH, – H, – NH2, – OH b. – H, – CH3, – Cl, – CH2CI c. -CH2CH3, -CH3, -H, -CH(CH3)2 d. – CH = CH2, – CH3, – C ≡ CH, – HArrange the following groups in order of increasing priority. Q.) -CH3 -CH2OH -CH2NH2 -CH2Br
- Rank the following groups in order of decreasing priority. a.−F, −NH2, −CH3, −OH b.−CH3, −CH2CH3, −CH2CH2CH3, −(CH2)3CH3 c.−NH2, −CH2NH2, −CH3, −CH2NHCH3 d.−COOH, −CH2OH, −H, −CHO e.−Cl, −CH3, −SH, −OH f.−C≡CH, −CH(CH3)2, −CH2CH3, −CH=CH2Order the following substituents from highest priority to lowest priority: CH3, OH, H,F. Use the Cahn-Ingold-Prelog priority system. a. F, CH3, OH, H b. H, CH3, F, OH c. F, OH, CH3, H d. H, CH3, OH, FRank the following groups in order of decreasing priority. −COOH, −CH2OH, −H, −CHO
- Arrange each set in order of decreasing priority using Cahn-Ingold-Prelog priority rules (1 for highest priority). d) _____-Cl, _____-OH, _____-H, _____-NH2 e) _____–CO2CH3, _____-CO2H, _____-OH, _____-OCH3(a) Draw a three-dimensional line structure of (5R,6Z)-6,7-dichloro-5-hydroxynon-6-enal. Place the aldehyde group on the right-hand side of your drawing.(b) Give the Cahn-Ingold-Prelog priority order of the four groups (-OH, -H, -(CH2)3CHO, -C4H5Cl2) at the C5 stereocentre (Highest 1 > 2 > 3 > 4 Lowest).please provide the machanisms of 1a, 1e, 1f
- Arrange the following group in order of increasing priority. Q) -OCH3 -CH(CH3)2 -B(CH2CH3)2 -HWhich group is of lower priority than –CH=CH2 according to Cahn-Ingold-Prelog rules. –CH=C(CH3)2 –C(CH3)3 –CH(CH3)2 –CH=CHCl a b c dShow how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show all reagents, and use curved arrows to show movement of electron pairs.