CUE COLUMN NOTES (A. Determine Stereoisomers it has ⑤ Identify any meso B compounds cl Br cl -c-c-c-c-¿- 1 CI C- | 2,4-Dichloro-3-bromopentane
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- is CH;CH, -C-H An isomer of || CH;CH, CH,-C-H CH;-C-CH; O CH3-O-CH2CH3 O CH3CH2CH2-OHh) i) + CH3CHSSCHCH3 CH3 CH3 Cl₂ [H] FeCl3 ? ?Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
- We’ll see in the next chapter that there are two isomeric substances, both named 1,2-dimethylcyclohexane. Explain.Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth methyl groups in __________ positions and one with both methyl groups in ____________ positions.H3C Cl \ / C=C / \ H2N I (R)-enantiomer (Z) isomer (S)-enantiomer (E) isomer meso compound
- compound CH3 CH₂0 CH3 — OH C- CH3 1 CH3-N - CH3 CH₂ ||| -C-H 01C- | NH₂ CH3 family esterGive typed explanationDZL Announcements - CHM240-201 ↑ Q X 82°F Partl app.101edu.co Organic Chemistry Draw all of the stereoisomers of 3-bromo-5-methylheptane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Select to Draw an Isomer x Select to Draw an Isomer Aktiv Chemistry Q
- d Copy the following structures into your notebook and determine the absolute configuration of each chiral center: H3CH₂C F Cl H H MIC1 CH3 ||| BI H₂CH₂C H H I ||||| CH₂CH₂CH3 "III COOH H OH OHQUESTION 7 Identify compound Y? H2 CH3 =-CH, Br2 4. Y Lindlar Pd racemic (2R,3R) and (2S,3S)-2,3-dibromobutane meso-2,3-dibromobutane racemic (2S,3R) and (2R,3S)-2,3-dibromobutane O 2,3-dibromo-2-buteneDraw the two chair conformations of the following trisubstituted cyclohexane. ndicate which of the two conformations is the most stable. OH Fl. ""CH3 Cl
