Rank the mechanistic steps. Not all steps will be used. methyl migration Start of mechanism Protonation of the alkene Formation of secondary carbocation addition of water to the carbocation deprotonation of the protonated alcohol hydride migration Formation of primary carbocation End of mechanism Answer Bank Addition of water to the alkene
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- Explain how and why rearrangements occurduring Friedel-Crafts alkylation reactions formingmore than 1 product. Also illustrate therearrangement reaction from the aboveexample.Rank the following alkenes by reactivity towards acid-catalyzed hydration. Most to least.In organic chemistry, an elimination process involves the removal of the hydrogen and a halide (i.e. dehydrohalogenation), in which they are ___ to each other, forming an alkene. syn-orientation co-periplanar anti-periplanar Z- orientation
- Heterocyclic compounds plays an important role in our daily life. They are mainly used in pharmaceutical and agrochemical products to name a few. 3. It is required to introduce a halogen group to a five membered ring, thiophene. Discuss the reaction mechanism involved in the reaction by selecting a suitable halogen group and analyze why a particular substituted product obtained after the reaction is predominant over the other possible product(s) with the help of reactions.Give the mechanistic Symbols CE1, E₂, SN, SN²) that are Con Sistent with Statemenst! most each of the following O Methyl halides react with Sodium ethoxide in eth and only by this mechanism In ethanol that contains Sodiumn ethoxide, tert-butyl bromide reacts mainly by this mechanism c) these reaction Con certed DJ these involve are mechanisms infere processes reactions mechanisms carbc cation intermedites E) Reactions proceeding by mechanisms are these SterospecificAn organic chemistry student reacted benzene (excess) with a racemic mixture of (S) and (R) enantiomers of 2-chloro-3,3-dimethylbutane in the presence of AICI3 followed by water. Which of the following represents at least 50% of the final product profile? [Note: more than one answer may or may not apply.] ok of d b a ok *** CI f
- The following reaction is Friedel-Crafts alkylation. Considering the mechanism for Friedel-Crafts alkylation, how would you explain the formation of this particular product? Either describe or upload image of the mechanism. AICI,Which of the following is capable of producing longer alkyne products? (A) Internal alkyne with NaNH2 and Alkyl halides B Terminal alkyne with NANH2 and Alkyl halides Internal alkene with NANH2 and Alkyl halides Terminal alkene with NANH2 and Alkyl halidesprovide the major profucts ( wrote "no reaxtion "if you think so) for the following reactions with correct stereochemistry. Please explain step by step with explanation
- Give reaction mechanism of all subparts in clear handwritten!Give the chemical mechanism for each reaction with the correct stereochemistry and regiochemistry for the major product.Below is a mechanism that represents the following single reaction sequence: a certain alcohol undergoes acid- catalyzed dehydration (conversion that involves the loss of water from the reacting molecule or ion) to form an alkene product. Write the IUPAC name of the product. Include E/Z stereochemistry. Hint: Name of the substituent of the product is similar to that of reactant. * :ÖH :O: :0: :O: 1-phenylpropanol oxonium ion H. нон Carbocation stabilised by resonance loss of water benzylic carbocation organic product + H-B Alkene formed ;B proton abstraction