Consider the compounds below; which is the most stable representation of trans-2-tertbutyl-cyclohexan-1-ol? A B C D OH OH OH tBu iBu tBu show work. don't OH give Ai generated tBu solution
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- Give the MAJOR PRODUCT/S of the following reactions. Include stereochemistry (wedges and dashes) asappropriate. Draw all major enantiomers and diastereomers.) Draw Strae hural formula cundinsed of the Hi compounds! al I chloro b) 4 Hydroxy - 4- methyl- using 2- propanone - 2- pentanene none Cyclo hexane diene I, 3 di 3 hydrexy butanal c) 2,2 - Dimethyl cyclo hexane Carbaldeliycde6. The product(s) of the following reaction dd blow di CH2-CH2 excess HBr is/are: CH2 CH2 heat Od Al () (A od Ocf D (CHPPCOK (CHPCON G)D CH;CH2OCH,CH3 HO CH;CH,CH,CH,OH and CH;CH,CH2CH,Br II H t mol boumol toubong soinm od o CH2-CHBR HO CH2 CH2 BrCH-CH,CH-Cн,ОН and BrCH,CH,CH-CH,Br CityCHCH COM III IV A) I B) П O II D) IV E) None of these HO CH CH'OH
- o o HCI Br₂ Br₂ H₂O Addition Stereochemistry 002) Predict the major product for each reaction. Indicate correct stereochemistry. a. b. H3C H3C HO ||||| HO ||||| CH3 ||||| Br H Br CH3 H NaOH NaOH thrive qode-tums ng uboiqyDraw tructural or or he ajor roduct f he eaction shown. CH3CH=CHCH3 Cl2 • Do not show stereóchemist in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. • Show product stereochem IF the reactant alkene has both carbons of the double bond within a ring. C. opy P. C. progress ChemDoodle (Previous Submit Answer Retry Entire Group 9 more group attempts remaining
- Need help on this question22 J Which one of the following alkenes is the most stable? H3C CH3 H3C CH3 H3C CH2-CH3 ÇH3 C=C H3C CH2 =CH2 H3C CH3 H3C H. IV I II II A O .B || .C O II DOll 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) Butylamine