Predict the major product formed in the following reaction. H. CH3 ༑ NaO CH, CH3 O,CCH H. ,OH HO. Η ིམ ི་ Η CH 1) H CH3 2) ., CH, Major product H H₂CCO₂ CH H ི་ ཡ ི་ CH; 3) Η Η CH; 4)
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- Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFPlease complete reactions in clear handwritten of all subpartsRearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangement
- Please help with this ochem mechanism... 1. Provide the stepwise mechanisms of the given reaction a) o,p-dinitrochlorobenzene + NaOHFill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?
- The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?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).Show the mechanism of the conversion of 2-methyl-1-propene (shown below) into PAN (peroxyacetylnitrate) and CO2 in the atmosphere
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