Q: What is a multi-step synthesis with intermediate steps to produce the following molecule?
A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…
Q: Use the appropriate reagent used in the reaction. (d),(e) please!!
A: Here we have to mention the appropriate reagent for reaction d and reaction e-
Q: Match each step with the description that best fits it. a)proton transfer b)nucleophilic attack…
A: Each step of reaction with following description are
Q: What is the needed reagent to perform the following reaction? OH ???
A: Alkenes are the organic compounds which contain atleast one double bond present in it. It can be…
Q: Nucleophilic substitution reaction""
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Q: Which alkyl halide in attached pair reacts faster in an SN1 reaction?
A: In SN1 reaction mechanism, the leaving group leaves first forming a carbocation which is finally…
Q: Identify (label) the electrophile and the nucleophile in the reaction and add curved arrows to the…
A: The specie which is electron deficient is known as electrophile and the specie which is electron…
Q: do the acetal forming mechanism
A: Given that, we have to show the mechanism for the formation of acetal.
Q: Explain why acetals do not react with nucleophiles.
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Q: Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw…
A: INTRODUCTION: Positively charged species is called as electrophile.It has an incomplete octet due to…
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Q: diffrentiate betwwen strong nucleophile and mild nucleophile.
A: A chemical species which donates an electron pair to form a chemical bond in relation to a reaction…
Q: + en
A:
Q: Draw the products of attached nucleophilic substitution reaction.
A: In chemistry various mechanism are studied. Some of important mechanisms are nucleophilic…
Q: nucleophile
A:
Q: Vhich is the better nucleophile in protic solvent? or O CI-
A: Solvent which gives hydrogen ions in solution called as polar protic solvent whereas solvent which…
Q: Which reacts fastest & slowest with m-chloroperbenzoic acid, why?
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Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…
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Q: What reaction sequence would lead to the following transformation? ?
A: here we are required to predict the reagent needed to carry out the following conversion.
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A: Structure of Compound and Product Formation mentioned in step-2
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Q: Rank the nucleophile strength of the compounds below from weakest to strongest
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Q: Explain why alkylation of an α-carbon works best if the alkyl halide used in the reaction is a…
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Q: Explain why quinuclidine is a much more reactive nucleophile than triethylamine, even though both…
A:
Q: This reaction takes place via a pinacol rearrangement. Draw curved arrows to show the movement of…
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Q: Show a reaction with nucleophilic substitution.
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Q: What reagentls) will perform the following miction?
A: The given reagent is a ketone. It belongs to the carbonyl family. the IUPAC name of the compound is…
Q: Determine which would be more reactive with a nucleophile
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Q: Alkenes and alkynes behave like . and thus attract, A nucleophiles; electrophiles B nucleophiles;…
A:
Q: Rank the species below in order of increasing nucleophilicity in protic solvent.
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Q: Explain the major step of a nucleophilic acyl substitution ?
A: The functional groups that undergo nucleophilic acyl substitutions are called carboxylic acid…
Q: Explain why alkylation of an a-carbon works best if the alkyl halide used in the reaction is a…
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Q: a. Which is a stronger base: RO- or RS-? b. Which is a better nucleophile in an aqueous solution? c.…
A:
Q: Propose a stepwise mechanism for this reaction. The bicarbonate ion will act as a base in the…
A: The given reaction is,
Q: Draw the products of attached reaction, and state whether the reaction is faster or slower than a…
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Q: Rank the nucleophiles in following group in order of increasing nucleophilicity. −OH, Br−, F− (polar…
A: The given groups are -OH, Br-, F- To find: The increasing order of nucleophilicity
Q: how to know whihc halide is more nucleophilic in a competition reaction
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Q: In the following reaction, which is the nucleophile? Which is the leaving group?
A: leaving group->A leaving group is a Molecular fragment that departs with a pair of electrons in…
Q: Identify the stronger nucleophile in the following pair of anions. HS− or F− in a polar protic…
A: A nucleophile has an electron density that can be donated.
Q: Devise a synthesis of attached compound from the indicated starting material.
A: In this reaction, we have to convert one isomeric form to another isomeric form. For this, we have…
Q: Rank the nucleophile strength of the structures from weakest to strongest.
A: In this question, we have to give Rank the nucleophile strength of the structures from weakest to…
Q: Which ester would hydrolyze faster?
A: The question is based on concept of Ester hydrolysis. We have to determine which ester undergoes…
Q: Determine whether attached nucleophilic acyl substitution is likely to occur.
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Q: Use any reagent, mention it and complete all reaction steps in clear handwritten please!
A: The reaction given is,
Q: Nucleophile of sulfonation reaction ?
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Q: What’s the stronger nucleophile in each pair?
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What
Synthesis of Nitrile compound can be easily done via substitution reaction of alkyl halide with KCN. Here you need 4 carbon alkyl halide therefore you can use Bromobutane as you starting material.
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- Draw the appropriate reagents and solvent above and or below the arrow necessary to conduct the following reactions.Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw curved arrows to illustrate the bond-making and bond-breaking processes.draw the reaction, including reactants, reagents and products.