For each organic compound in the table below, enter the locant of the highlighted side chain. compound CH₂ CH3CH₂-CH-CH3 CH3 I CH3CH₂-C- CH₂ CH3-CH CH3 CH3 - CH₂ locant of highlighted side chain X 0 0 5
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- For the substituted cyclohexane compound shown, identify the atoms that are trans to the bromo substituent. I CH3 Br J HD HCI НА FF HB НОЕ HG CI Identify the atoms that are trans to the bromine. A В D E F H KWrite the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule i H3N + NH3 common name (not the IUPAC name) H N NH ☐ شهدة + NH3 | ☑For the substituted cyclohexane compound shown, identify the atoms that are cis to the hydroxyl (OH) substituent. ECH3 BrH A H F F- C -HJ HO GF ČI K Identify the atoms that are cis to the hydroxyl. A В E F G H K
- Provide a systematic name (IN SMALL LETTERS except for E/Z and R/S, NO SPACES) for each of the given compounds.Draw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexaneWhich one of the following equations is incorrect? OH CH3CH₂CH₂OH Cr₂O7² H₂SO4 CH3CH₂C=0 a) OH H 1 Cr₂O7² | CH3CH₂C=0 CH3CH₂C=0 b) H₂SO4 O O || H+ CH3C-OCH3 + H₂OH, CH₂C-OH + CH3OH c) O || CH₂CH3 CH₂C-ONa NaMnO4 NaOH d) a O O C Jd
- SNI or SN2? Draw the substitution product for each of the following (if there is one). Br Br H NaOCH3 OTS Br CH3OH NaCN H₂O GEthambutol is an anti-tuberculosis medicinal agent with two stereogenic centers, as shown in the given skeletal structure. It has 15, 2S configuration at its stereogenic centers. Redraw ethambutol, showing the correct configuration at each of the stereogenic centers. OH H fil N H 2 OH - Click and drag to start drawing a structure. C C С X Ś CX è1. Name compounds by IUPAC nomenclature CH₂CH-COOH a ОН 2) Find all of the heterofunctional compounds among following: ОН 2 сн, -ен, -с NH, OH COOH CH-OH CH,COOH e b COOH H-C-OH н-с- -ОН COOH -СООН f с H₂C-C-CH₂ 0 COOH HO-C-CH,COOH CH,COOH CH2-CH-CH2; OH ОН ОН g d ОН HOOC–C–CH,COOH ОН HOỌC –COOH б ONa
- Draw a structural formula for the substitution product of the reaction shown below. H/ ● (CH3)3C |YY Br ΔΟ H Na • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one stereoisomer of product is formed, draw both. Separate multiple products using the + sign from the drop-down menu. • Products that are initially formed as ions should be drawn in their neutral forms. SH acetone [FWhich compound is a meso isomer? Br H-CH₂ H₂C H H -Br CH3 A Br -H H- -Br H- CH₂ B CH₂ -Br H -Br H₂C CH3 с Br Br D I -CH₂ Br- -CH₂ -H H₂C- Br hill.com:80/olcweb/cgi/pluginpop.cgi? E onClick="window.open('http://highered.mcgraw- (29.0K)Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the acetoxy with the para position in phenyl acetate. phenyl acetate ● CH3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one. Sn [F ?