Q5: What would be the product of the following reaction? Explain. 1. Mg turnings 2. CO2 Br ? Ether Q6: Which of the following can be turned into Grignard reagents without reacting with themselves? Explain your thinking. Br Br CI N HO H. Br ZI
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- draw the potential products in the space below, for the halogenation (with heat/UW light) reaction:Please help me with the organic chemistry problem below: Consider the reaction below: (Check the attached image) (it is between Furan and maleic anhydride, a DIels-Alder reaction) a) Will this reaction for an endo product (with a melting point of 80-81 degrees) or the exo product (with a melitng point of 114 degrees)? b) Carefully explain why the product must have been formed the way it did (exo or endo). c) Provide a mechanism for this reaction.What happens to the rate of an SN1 reaction under the following conditions? [RX] is halved, and [:Nu−] is doubled
- Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productBelow 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?Organic Chemisrty study guide help. I need help with this question and have no idea how to do it. It says, "Draw all possible chlorination products of the following reactions:"
- could someone help me by telling me which out of both of these pairs would react the fastest with an SN2 reaction and why? Thank you, I just need help with an explanation :)Examine the nucleophilic substitution reactions shown below:3) If the product of an SN1 or Free radical reaction contains a stereocenter then a _______________ mixture occurs. Complete the sentence above and explain why this occurs. 4) List and explain the 3 steps of a free radical reaction.
- 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?Find the products for these two reactions. Make sure to include relevant hydrogens, deuteriums and stereohemistry.please answer part two (Please answer "What is BP of the solvent, and the authors state... why is that important"). thank you "The 3-Sulfolene is the prime molecule used for synthesis for the 1,3-butadiene molecule. The mechanism involves breaking of two C-S bonds in 3-sulfolene to generate 1,3-butadiene in the presence of heat. The reaction can be shown as below: This reaction is a type of pericyclic reaction that involves breaking and making of bonds in a single step and hence there will be no intermediate formed. The solvent used here is water." https://www.bartleby.com/questions-and-answers/3-sulfolene-a-butadiene-source-for-a-diels-alde-synthesis.-please-be-prepared-to-take-a-quiz-on-this/8bf8358d-dbdf-46f9-97db-6f744d66c0cd