Consider the organic product in the drawing area below. Click and drag to start drawing a structure. + Add one or more lone pairs G છે P Oyes O no Can this product be made by an addition reaction with one alkene reactant and no more than one small molecule reactant? If you said the product can be made by an addition to an alkene, would the reaction need to create mostly Markovnikov or mostly anti-Markovnikov product? Finally, if you said the product can be made, draw the alkene reactant and any necessary small-molecule reactant on the left-hand side of the reaction above. Remember to add no more than one small-molecule reactant. Note for advanced students: you don't need to draw any catalysts, required reaction conditions, solvent, et cetera. Just the alkene and any small-molecule reactant. Also, your proposed synthesis should not rely on any carbocation re-arrangements. Markovnikov anti-Markovnikov Br

Consider the organic product in the drawing area below. Click and drag to start drawing a structure. + Add one or more lone pairs G છે P Oyes O no Can this product be made by an addition reaction with one alkene reactant and no more than one small molecule reactant? If you said the product can be made by an addition to an alkene, would the reaction need to create mostly Markovnikov or mostly anti-Markovnikov product? Finally, if you said the product can be made, draw the alkene reactant and any necessary small-molecule reactant on the left-hand side of the reaction above. Remember to add no more than one small-molecule reactant. Note for advanced students: you don't need to draw any catalysts, required reaction conditions, solvent, et cetera. Just the alkene and any small-molecule reactant. Also, your proposed synthesis should not rely on any carbocation re-arrangements. Markovnikov anti-Markovnikov Br

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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rks Window Help = A ALEKS- Jacari Johnson - Learn O PRINCIPLES OF ORGANIC CHEMISTRY Classifying organic reactions Classify each of the following as either a substitution, elimination, or addition reaction. O CH3 HO-C-C-CH3 + NH3. CH3 CH3—O–CH2–0–CH3 + H2O Explanation CH3 CH3-CH-CH₂-CH₂-Br CH3 CH₂-CH-CH3 CH3 CH₂=C-CH₂-OH+Br2 Check A H* DBN Pt/Sn catalyst A O CH3 HẸN-C—c–CH3 + H2O CH3 CH3-O-CH₂-OH + HO-CH3 CH3 CH3—CH—CH=CH2 + HBr www-awu.aleks.com CH₂ CH3-C-CH3 + H₂ CH3 Br-CH₂-C-CH₂-OH Br O substitution O elimination addition O substitution O elimination O addition O substitution O elimination O addition O substitution elimination O addition O substitution O elimination O addition Ć Cher X
Draw the organic product structure formed by the reaction sequence. Draw the product. Select Draw Rings More Erase H 1. B2H6, diglyme 2. NaOH, H,O, Н-О2
4:32 Done 13. Hydrogenation of glyceryl trioleste, a triacylglycerol made from three oleic acids and glycerol, Converts the ester group to a ketone group. 14. The products of the acid catalyzed hydrolysis of a fat are A) the esters of fatty acids. the ester group to a carboxylic acid group. the alkene group into an alkane group. converts the ester group into the alkene group. B) fatty acids and glycerol. C) salts of fatty acids. D) salts of fatty acids and glycerol. E) phospholipids. 15. In the list below, which lipid type is most soluble in water? A) triacylglycerols B) glycerophospholipids C) oils D) steroids E) waxes (+) CHEM 6 o 16. The type of lipid that gives a cell membrane its shape is a A) triacylglycerol. B) glycerophospholipid. C) prostaglandin. D) bile salt. E) WEL 17) Which of the following contains a-1,6- branches? A) amylose B) glycogen C) cellulose D) sucrose E) maltose A LANG 4 18. Lipids are compounds that are soluble in A) distilled water. B) normal saline solution.…
CH=CHCN 3-phenylpropenenitrile Electrophilic substitution on 3-phenylpropenenitrile occurs at the meta position. Draw resonance structures to show how the ring is electron-poor at the ortho and para positions. ● • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the → symbol from the drop-down menu.
Draw structural formulas for organic products A and B in the window below. H₂O Mg ether ● ● ● H3CC=CH₂ Br *8 Draw only products having the organic portion of the original alkyl halide. Draw carbon-lithium bonds using the single bond tool. If a structure has a copper-lithium bond, do not draw the lithium. Separate products from different steps using the → sign from the drop-down menu. ? A Ⓡ ChemDoodle B Sn [F
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Criteria for satisfactory score Reactants, products, and reagents that complete a reaction scheme must specific compounds, not generic categories. Reagents and structures must be valid Lewis structures. Tasks 1. Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below. 2. Draw the mechanism of tautomerization (line 3).
Are these substitution, elimination, addition or rearragnement?
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Topics] [References] Draw the structure(s) of the major organic product(s) of the following reaction. ● ● ● ● ● + ● Br . If no reaction occurs, draw the organic starting material. Draw one structure per sketcher. Add additional sketchers using the drop-do Separate multiple products using the + sign from the drop-down menu. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the g Do not include the amine from which the enamine was derived. ? 1. dioxane / reflux 2. aqueous HCI Ⓡ ChemDoodle ▼
takeAssignment/takeCovalent Activity.do?locator=assignment-take [Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. 0 7 H3C • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. + • Do not include counter-ions, e.g., Na+, I, in your answer. . In cases where there is more than one answer, just draw one. CI -8) CH3OH 8) ₁ [F + ? ✩✩ ✰ ✰ C
Predict the product of this organic reaction: OH CH3-C-CH3 CH3 [0] P + H₂O Specifically, in the drawing area below draw the condensed structure of P. If there isn't any P because this reaction won't happen, check the No reaction box under the drawing area. Note for advanced students: you can assume the reaction is run under mild conditions. Click anywhere to draw the first atom of your structure. X Ö Ś