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- Which carbocation will form after the carbocation below undergoes rearrangement? || I IV + 8d8d || ||| IV VWhat is the major elimination product obtained from the following reaction? Br ||| IV NaOMe MeOH || ||| IVRank the compounds in order of reactivity toward nitration with HNO3: benzene 2-methylfuran thiophene Most reactive Least reactive Answer Bank 3-methylthiophene
- 24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IVDraw the major organic product for the reaction. H₂O cat. TfOH -H Select |||| Draw Rings с H 0 MoreConsidering stereochemistry, draw the resulting E2 elimination product when H, is removed. H₂ H All H Br |||| X AJ U: S G
- Predict the major product for the reaction. HCI Draw the major product. Select Draw Rings C H Cl |||| MoreRank the following nucleophiles from weakest to strongest (e.g. least reactive to most reactive). 1 O OI<|| < |||-Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will form the aldol dehydration product. 10% NCH 5°C Step 1: add curved arrows. Select Draw Templates Mar |||||||||||| M Complete the mechanism for the dehydration reaction by adding missing honds and curved arrows. Draw the aldol dehydration product in the last step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure 3 Ć НО Era Q2Q Step 3: complete the structure of the product. Select Draw Templates Mar XTZ ? 10-1 Q2Q Step 2: complete the structure and add curved arrows. Select Draw Templates More ||||||| Era AND 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 NH₂Plastic 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)?Predict the major product for the reaction. H Cl₂, CH3CH₂OH Draw the major product. Select Draw /||||||| Rings C H Cl More O EraseSEE MORE QUESTIONS