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- [IV2] Instructions: Follow the flow of electrons indicated by the curved arrows in each of the following reactions, and predict the products that result: (refer to the photo below)Please help with this ochem mechanism... 1. Provide the stepwise mechanisms of the given reaction a) o,p-dinitrochlorobenzene + NaOH2-Methylpropane have more than one kind of hydrogen and will generate 2 different products with bromination in the presence of uv light. t or f
- When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.Please provide the answers in each situation. 1. Which compound/s will react with Br2 in water under light conditions? (answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (answers may be one or more)d. Reaction with CH3MgI (excess), ether; then H+/H2O e. Reaction with LiAlH4, ether; then H+/H2O f. Reaction with DIBAL (diisobutylaluminum hydride), toluene, low temperature; then H+/H2O
- LDA/THF, 78°Clongrightarrow Predict the major product of the following a- halogenation/a - alkylation reactions under the given reaction conditions.What reagent(s) is needed to complete the transformation below? Options: BH3, then NaOH/H2O2 HBr with peroxides (ROOR) Br2 in H2O Br2 in HOCH3(SYN) The reaction in Problem 10.48 produces a mixture of ethers rather than the desired ether exclusively. Starting with the same two alcohols given in Problem 10.48, show the sequence of reactions that would need to be carried out to produce (1-Ethylpropoxy)cyclopentane as the exclusive ether
- Reaction of (CH3)3CCHO with (C6H5)3P=C(CH3)OCH3, followed bytreatment with aqueous acid, affords R (C7H14O). R has a strong absorption in its IR spectrum at 1717 cm−1 and three singlets in its 1H NMR spectrum at 1.02 (9 H), 2.13 (3 H), and 2.33 (2 H) ppm. What is thestructure of R?2-butanol + NOx + hv (assume the carbon-hydrogen bond on the carbon adjacent to the carbonwith the alcohol group is the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).Provide the answer if the compounds will react. 1. Which compound/s will react with Br2 in water under light conditions? (explain each compound; answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (explain each compound; answers may be one or more)