Question 1. Provide a full, rigorous mechanism for the transformation below. Include all possible intermediate and resonance contributors. Rank the products in terms of their likelihood of being formed. Explain your reasoning. F₂C H₂C SO₂ H₂SO4
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- Please give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!draw the potential products in the space below, for the halogenation (with heat/UW light) reaction:The reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followed
- draw the major organic product generated in the reaction below. Pay attention to Regio and stereochemical detailWhy we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added. b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination. c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5. 5. There will be a mixture of products because there is no selectivity for a major product.as a follow-up question can explain this mechanism
- Plan out a proposed mechanism for the “new” reaction below.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?The question is: "Draw the curved arrow mechanism for the reaction between (2S,3S)-3-methylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms" I attached screenshots of the picture of the atoms below. What type of reaction (SN1, E1, SN2, or E2) would the reaction be, and how would these molecules interact? The question asks for multiple steps so I am guessing it is either SN1 or E1, but what is the reaction mechanism?
- ( complete the reaction with mechanism , do 2st one )Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?