Which mechanism is incorrect? They all seem correct as the halides are attached to the secondary carbocation in (a) and (c), and the halides are attached to the primary carbocation/end of the organic molecule in (b) and (d). Should the answer be (e)?

Q: Please drauuthe Mechanism for+this polumentzoben

A: Chain initiation step include,

Q: Which of the following mechanisms is drawn correctly? Remember to check arrows, formal charges,…

A: This reaction follows E1cb mechanism i.e, Elimination Unimolecular conjugate base, that first base…

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A: The given mechanism is the general mechanism of electrophilic addition of alkenes and alkynes.

Q: Enol form in the mechanism of * halogenation is present.step Fast Slow Both

A: Answer :- Enol form in the meachnism of halogenation is present fast step.

Q: Please correct them and use the structural form the way it's written. Whether a mechanism…

A: E2 mechanism transition state requires an antiperiplanar orientation of the leaving group. Hence,…

Q: for both pics, can you please see what the arrow notation is in the structure for the reaction…

A:

Q: d. Consider the following secondary halides. Changing the leaving group from fluoride to bromide…

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A:

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Q: shown

A: Dear student, I have given answer to your question in the image format.

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A:

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A: Interpretation: We have to write the product for the following reaction.

Q: Give the missing r. mechanism throug not necessary.)

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A:

Q: Draw out the mechanism for the reaction between any peroxyacid and cyclohexene.

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Q: Is the given mechanism is correct or not,please confirm?

A: Yes, the above reaction to acid catalyzed ring opening of epoxide. So, the first step is attack of…

Q: Br NBS, HV.

A:

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A: The given compound is an alcohol and we need to check the possible fragments.

Q: alternate route or reaction? I

A: Your proposed reaction scheme is ok. Only one problem is that F being electron withdrawing group,…

Q: de, what are the products (=

A:

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Q: provide the complete reaction mechanism for each of the following steps shown in the figure

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Q: Provide the full mechanism of this SN2 reaction.

A:

Q: Consider the following Diels-Alder reaction: a) Draw a detailed mechanism for the reaction and show…

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A:

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Q: Explain why substitution is difficult on accomplish on the benzene ring?

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A: The reaction given is,

Q: Can you draw the mechanism specifically for the cleavage part,

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Q: For each of the alkyl bromides, do think it is likely to form the you substitution or elimination…

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Q: Which of the following reactions in each pair will occur faster?

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Q: Fill in the blanks: The rate of the SN1 reaction depends on the and therefore involves kinetics.

A:

Q: Of the following, which correctly uses curved arrows to display a possible step in a radical…

A: Radical is a single electron species. Hence, one headed arrow must be used.  For anionic mechanism…

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A:

Q: BY ANALYZING THE STARTING MATERIAL AND THE PRODUCT(S), THE FOLLOWING REACTION IS AN EXAMPLE OF WHAT…

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A:

Q: ? CH, Hint Remember that overalkylation is a problem when it comes to Friedel-Crafts

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A: Favorskii rearrangement is base catalyzed reaction in which the alpha-halo carbonyl compound form…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.