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- Which carbocation will form after the carbocation below undergoes rearrangement? || I IV + 8d8d || ||| IV VFor esch of the following two reactions draw the major product. Br,, hv KMNO, heatWhat is the product of the following sequence of reactions? D | NaOH NaNH2 H3O+ || ||| explain each steps..explanation needed. don't give Handwritten answer IV NH₂
- Predict the major product for the reaction. HCI Draw the major product. Select Draw Rings C H Cl |||| More• Draw the curved arrow mechanism for the following reaction. o Show all electrons, spectator ions, formal charges, and intermediates. o Only account for the products shown. • Account for any stereochemistry and regiochemistry provided. Overall Reaction 1. 1 equiv CH₂MgBr, ether 2 water workup OH + enantiomerQ3/ Draw a stepwise detailed mechanism that illustratés how four organic products are formed in the following reaction OCH, CH;OH HCI OCH
- 4) Give the correct product with the correct stereochemistry. Me Me 5) Give the major product. hv HCI OCDraw the products formed when each ester is treated with lithium hydroxide and water. Reaction A Select Draw Rings More CH3CH₂CH(CH3)OC=OCH(CH3)₂ LiOH H₂O |||||| HO 3 Ć H O OH Li Erase Q2QDraw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction. CI OCH, CH;OH + HCI OCH3
- Draw the major product of the reaction shown. OI O III O IV OV eTextbook and Media OMe = CI = ||| oto IV V ||Draw the mechanism ffrom benzaldehyde to this using: i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+, H2OPlastic 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)?