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Q: 1) 3- Methyl-2-butanol will react with H2SO4 to give two isomeric alkenes. Write suitable reaction…
A: Given Reactant = 3 methyl 2 butanol and H2SO4 Major Product = IUPAC name of each product = ?
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- Illustrate the Reaction of a Radical X• with a C=C ?The following radical-initiated reaction with HBr produces a formal Anti-Markovnikov's rule product. Provide a curved arrow mechanism, making sure to use single headed arrows and drawing all intermediates. Only initiation and propagation steps are needed. Termination does not need to be included. Part of the initiation step is provide for use to generate an OH radical.If you want to disrupt the ability of radicals to generate more of themselves, particularly in scenarios where they could be harmful like auto-oxidation, you need to find a suitable scavenger reagent. Such materials, known as antioxidants, succeed when they can lead to a new, more stable radical species that terminates the chain without reacting, or by further consumption of reactive radicals to generate additional non-radical species. Which species(s) is or are radical-scavenging reagent(s)? * I just II, only III, only IV, only I and II, only II and III, only III and IV, only
- In theory, there are only three inequivalent hydrogens in this molecule that could be substituted by Br in a free radical bromination – circle them. Put an asterisk to mark the one most likely to be substituted first.i wonder which number is the most reactive and the least reactive in sn2 reaction? can you rank them?Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)
- Draw the most stable radical that can result from cleavage of a C–H bond in attached molecule.What are ALL of the products when adding hexa-1,3,5-triene and bromine in CCl4? I know how to get the major product (both bromines next to each other due to epoxide) but don't know how to get to the other major and the minor product?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.
- From the given structure, indicate the most stable radical.Radical allylic bromination is also something that although I understand resonance structures I can't quite grasp how to approach problems like this. Thank you in advance for the help this site has been a lifesaver for my ochem understanding.In the presence of a radical initiator (Z•), tributyltin hydride (R3SnH, R = CH3CH2CH2CH2) reduces alkyl halides to alkanes: R′X + R3SnH → R′H + R3SnX. The mechanism consists of a radical chain process with an intermediate tin radical: This reaction has been employed in many radical cyclization reactions. Draw a stepwise mechanism for the following reaction.