• . HO CH3 17 13 CH3 10 cholesterol You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. 1.03 2. Zn, H₂O* . Should I you want to restart the exercise, the drop-down menu labeled == starting points == can be used t HO H3C CH H3C -CH3 4 [F ?
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- Draw the structure of the following three isomeric acid chlorides with chemical formula C6H₂CIO. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Consider E/Z stereochemistry of alkenes. • In cases where there is more than one answer, just give one. Acid chloride #1: cis-3-methylcyclobutanecarbonyl chloride //. | [ ]# ? ChemDoodleDraw a tetrahedral representation of the (2S,3R) enantiomer of 2,3-dibromopentane. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. **8 MAVIL On [] ? Ⓡ ChemDoodlereactions. Be sure to show any significant stereochemical details. (a) I. Nall. CS 2. CH,I 3. heat (b) 1. BULI, LICI 2.MeCu(CN)LI (c) CH, Zn-Cu CH,l,, ether (d) CH,CO,H LOET (e) Br Zn, THO.
- Draw a structural formula for 2-methylbutan-2-ol. • You do not have to consider stereochemistry. **** Sn [F ? ChemDoodleⓇWhich of the following statements is TRUE? H2N Mẹ. F Ph Select one: O a. This molecule is called (1S,2R)-2-fluoro-1-phenylpropan- b. This molecule is called (1R,2S)-2-fluoro-1-phenylpropan- C. None of others O d. This molecule is called (1R,2R)-2-fluoro-1-phenylpropan-I e. This molecule is called (1S,2S)-2-fluoro-1-phenylpropan-1Chemistry Hi I need some help with my homework, thank you for your help! Problem Set 9 CHM 3150 Organic Chemistry II Name: Topics covered: Kinetic vs. thermodynamic control of diene additions, Diels-Alder reaction Predict the major product for the following Diels-Alder reaction. Clearly indicate the stereochemistry if there any. 1 a. b. C. d. CH,0. CH;OCH, O,N H. Which diene and dienophile would react to give the following Diels-Alder přoduct? OCH 3. Provide the major product of the below reaction. Identify the product if 1,2- addtion product (KIN Pdt) or 1,4-addtion product (TD pdt). HBr -78 °C Briefly explain why 1.2 product of the above reaction is kinetically favored (KIN Pdt)?
- Draw a tetrahedral representation of the (2S,4S) enantiomer of 2-bromo-4-chlorohexane. O Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. [ ] در ? ChemDoodleⓇ✓ C n https://education.wiley.com/was/ui/v2/assessme... A Macmillan: The Bed... Ⓒ How To Write Biolo... a Amazon.com 150 E... How To Fight Aging... ← Chapter 4b Question 25 of 25 -/1 = : Draw Haworth projections for cis-1,3-di-tert-butylcyclohexane and trans-1,3-di-tert-butylcyclohexane. One of these compounds exists in a chair conformation, while the other exists primarily in a twist boat conformation. Offer an explanation. Part 1 Select all correct statements. OH t-Bu corresponds to a Haworth projection of trans-1,3-di-tert-butylcyclohexane. t-Bu H C t-Bu t-Bu M corresponds to a Haworth projection of cis-1,3-di-tert-butylcyclohexane. H H Vi ΠΗ t-Bu corresponds to a Haworth projection of trans-1,3-di-tert-butylcyclohexane. Q. H Type here to search O 1x PrtScn F2 @ ▬▬ ― 1 Q A 0 t-Bu 2 W S # 3 E F3 $ 4 R D F % 5 T F5 A 6 10 F6 Y G H & 7 F7 U H e Home 8 F8 1 ^ V End 9 K F9 Mu OAktiv Chemistry Kinesis scolarship app.101edu.co I Meliora! - FAOnline Draw a product that could be formed when 1,3-butadiene reacts with (E)-2-butenedinitrile. Include any relative stereochemistry. NC Drawing CN Neuromedicine -... Version: 1.76.3 + production Neuromedicine -... Problem 30 of 18 Atoms, Bonds and Rings Charges Study Abroad Draw or tap a new bond to see suggestions. Applying to Medic... Undo Remove Drag To Pan Reset Submit Done +
- chem 534 cha Hư OAC H please show stereochemistry H₂ COCH ? H CO₂CH3 O Ac 2. + ? hv 9 40°C 3. H₂ C 4. 0°C Catq Q-0 + [6+4] NGC ?. لك 5. [ V-CO₂CH3 + II NCCN [4+2] C6H5 6. 2 C6H5SOlve the attached]>90% e.e. TSOH (cat.), CH,Cl2 then workup racemic но mostly one diastereomer ]5:1 diastereomer mix product after these transformations >90% e.e. 2) a) NANH2, THF, -20 °C b) OHC-CH,CH3 c) workup ]racemic mostly one diastereomer 3) NaH, MegSi-CI, then workup ] 5:1 diastereomer mix product after these transformations