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- 1. Which absorbs at higher frequencies: a C-H or C-D bond? Explain. 2. Predict which alkene will predominate at equilibrium. Explain.Determine and draw the product of the following reactrans ,write in any added hydrogens. 1,2,3,4,1bDraw the structure(s) of the major organic product(s) of the following reaction. NH₂ O₂N NaNO₂ aqueous HCI at 0°
- 1.Draw the structures of all 3 resonance hybrid forms of the benzenonium intermediatefor both o and p attack for the case of activating groups an indicate which one in eachcase is the most stable form.Draw the structure of all 3 resonance hybrid forms of the benzenonium intermediatefor m attack in the case involving a deactivating group. 2.Halogens are deactivating groups but direct electrophilic attack at the o and ppositions. Why is this the case?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)?
- In the reaction between 1-methylcyclohexanol with hydrogen bromide to form 1-bromo- 1-methylcyclohexane and water, a) How would the rate be affected if the concentration of HBr is doubled? pls. draw involved reactionsOrder the following compounds from least reactive to most reactive with MeMgBr.Provide the complete the following mechanism for the reaction below. You must include appropriate arrows,intermediates, and formal charges. Please answer fast i give upvote
- ! ( plz ans with proper explanation , aslo give mechanismDraw the stucture of the organic reactant/s or product/s of the following reactions. ASAP please.Provide the curved arrow mechanism for the reaction of the compound shown below treated with Cl2/FeCl3. Include transition states and the major product. I apprecitate the help