Select the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN 1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Br H₂O Select Draw Templates More CH 0 Erase
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- For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Br H CISelect the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN1 reaction. Include wedge‑and‑dash bonds and draw hydrogen on a stereocenter.Predict the organic product for the reaction. OH K₂Cr₂O7 H₂SO4 :ÖH acetone Select Draw Templates More H₂CrO4 |||||||CH 0 Add four curved arrows to complete the intermolecular mechanism that forms the oxidized product. Note that potassium dichromate in acid is in equilibrium with chromic acid used. 3 Select Draw Templates More H H 0: C H H Cr 0 : OH Q : 0:
- by Macmillan Learning Select the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. 4 Br R F 888 V % 5 T F5 G H₂O B F6 Y MacBook Pro H Select & 7 / || ||| ▼ 3 C U Draw N 8 J 20 Templates DII M ( 9 More C H 0 K H дв F10 L P command 2 Q S Erase ? } optionDraw the major organic product(s) for the Friedel-Crafts acylation reaction. CH3CH₂CH₂COCI FeCl3 Select Draw Templates More III C H O ClDraw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reag
- 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. CI + H₂N • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. OH • Do not include counter-ions, e.g., Na+, I¯, in your answer. • In cases where there is more than one answer, just draw one.Select the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN 1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. OH HBr Select Draw Templates More ////// C H Br Erase QQ QAdd curved arrow(s) to draw step 6 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. Use the +/- tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds. F H C N 0 P SF OH ہیں۔ ہوم CH3 CH3 CI Br CH3 H.C CH3 H₂C Y\Z++++ - 1
- 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. CH3OH H3C CI • • • • 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.Select the correct IUPAC name for the following organic substrate, including the R or S designation where appropriate, and draw the major organic product(s) for the SN1 reaction. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Select Draw Rings More Erase HBr HO,Predict the products for the following reactions by showing complete reaction mechanisms. Also, identify the nucleophilic attack, loss of leaving group, proton transfer, rearrangement in the mechanism steps. Show curved arrows in the reaction mechanisms 1- 2- COCH3 NaBH4/H₂O COCH 3 1. LIAIH4 2. H₂O