last answer is correct.
S. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s)....
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
4. Reaction Fill-ins! Predict the product(s) OR starting material of the following reactions. Remember Hydride shifts are possible if when a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes. H2SO4 (cat.), H20 а. 1.4-product 1.2-product Br Br HBr b. Br Major product Minor produt Minor product HCI C. 1,2-product 1,4-product HI он MAJOR prod Minor prod. e. Draw the FULL electron-pushing mechanism for the reaction in part a above, INCLUDING ALL resonance...
4. Reaction Fill-ins! Prediet the product(s) OR starting material of the following reactions. Remember, Hydride shifts are possible ifwhen a more stable carbocation can exist (depending on reaction mechanism)! Put your answers in the indicated boxes H,SO, (cat), H,о а. 1,2-product 1,4-product Br Br HBr b. Br Minor produt Major product Minor product HCI C. 1,2-product 14-product HI Он MAJOR prod. Minor prod e. Draw the FULL electron-pushing mechanism for the reaction in part a above. INCLUDING ALL resonance contributors....
Draw the missing major organic product(s), starting material(s), or reagents for each of the following reactions (DO NOT WRITE +EN AS A PRODUCT (ie draw everything out!)! And remember stereo and regiochemistry.) Assume reagents are in excess unless otherwise indicated. **To make things simple, I indicated what is needed for each section! Please don't just put the answers, but explanations as well on why. Thanks! a) draw the starting material for this reaction. b) draw the product for this reaction....
8. [18 pts) Provide the expected organic product(s) from each of the reactions below. Ignore the stereochemistry. No mechanism required! (3 points for each organic product, switching the major and minor will be penalized) a. Major: NaOCH; E2 Br b. Major Minor OH E2 Br 3 products in total CH,OH ΕΙ 6. 19 pts] For each of the following reactions, give the organic product(s), and include the stereochemistry when applicable. No mechanism required! (3 points for each organic product) a....
Draw the structures of the expected organic product(s) formed in the following reactions including correct stereochemistry. If more than one product is possible draw all products and write major or minor product where necessary. Indicate what the mechanism of the reaction is. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'. DMF = dimethyl if ormamide, CH_3 CN = acetonitrile
suggest the major product(s) for the following reactions. specify the stereochemistry clearly and write "racemic" for a racemic product. Br КОН heat BH3, THF NaOH, H2O2 NaN3 DMSO Br HCI SOH HBr
Draw the structures of the major product(s) of the following reactions. Please specify stereochemistry whenever applicable acetic anhydride acetic anhydride H3PO4 H3PO4 ferrocene Br2 2 NaNH2 2HBr H2 2 NaNH, Pd/CaCO3 PboAc 4. Wrich of the follow molecules is more stable? Explain briefly. (5 points) 102 1
3. Predict the majoe product(s) for the following reactions. Show the stereochemistry of the product(s) when applicable. HCI (1) Hg(OAc)2 (2) NaBH4 (1) BH3 THF (2) H202. OH Br, Br2. H20 Pt (I) CH3CO3H (2) H,O+ (2) DMS HBr ROOR
II. Reactions: Predict the major organic product(s) or write the appropriate reagents/starting materials for the following reactions. Indicate stereochemistry and regiochemistry when appropriate. Indicate reactions that are expected to result in a racemic mixture of products DBr 1. Н.О, CHCI он HSO, heat кон 1) вн, THF 3. 2) H202. HO 1) Hg(OAc)2, CH,OH 2) NaBH, OH 5. Br2 SH 6. HIO4 OH THF, H2O "он III. Synthesis: Starting from the alkenyl bromide below, devise a synthesis that produces the...