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- A) Draw the prodocts of the folowing reactions taking into ccount the given moleciar formukas: HO NAOH CaH Br Ho NOOH 1B Why dipperent products are dbtained in te above reactions? 1C. 2- metnoxyethanol is a Sobstance Osed to meit ice and Snow..which reagent make it from epoxide? Draw a detailed mechonism, induding a hall - electron transition and intermediate Can be Used to products f the reaction.2. Which of the following would give a meta product when submitted to EAS reaction conditions? OA OB OC OD OE OF A B C H CF3 E F CI HOWhat is the predicted product of the reaction shown? ОТ O II O ||| O IV OV Н Na2Cr2O7/H2SO4/H2O IV || ОН ОН овог H V Ш OH ОН
- V. @Given the following mechanism fer me Y OCHS NaOH reaction show the detailed conversion of A to B •OCN3 CH3OH. OH (A) (B) c Ⓒ using the same detailed mechanism instead of cyclonexare ring as shown in product. B, propose and fer a product wil a cyclopentane ning instead of a cyclohexane viny. Ⓒ Exploumpand I with why campand (B) is preferred over the campanay campand with a cyclopentake ring..NaOMe MeOH A B D E F What are the two starting materials? ofPlastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?
- The following reactions are unlikely to provide the indicated product in high yield. What is wrong with each?The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?ab provide d remo gy nthesi's ANDA Forcward Synthesi s for the fouowing tano Foma ton from the provided startung matenon (some of whos e carbon atoms mustbe Integrated into the pro duct -i.eyou can't sust draw the produet as the Other reagens. Mather reagent and any. 'NO mechandsms required: Br Br
- Give the organic product: OA OB OC NO₂ A CI 6 NO₂ NO₂ B + CH,-SH S-CH; CH3-$ C ? S-CH; DWhat starting materials are needed to synthesize each azo compounds O2N H2N- -N=N- CI но -N=N- -CH3 I0 Fill in the reagent or starting material needed or product in each reaction a) CgH;CH;CH;CH2Br CGH;CH;CH;CH¿NH2 b) C,H;CH;CH;CH2CONH, CH,CH;CH;CH;NH2 HCI P-CH;C,H4NH2 NANO2 P-CH;C,H&NH2 HCI/H;0 P-CH3C,H4NH2 CH;COCI4) Give the correct product with the correct stereochemistry. Me Me 5) Give the major product. hv HCI OC