In the following reaction, which is the nucleophile? Which is the leaving group?

Q: Compare the following pairs of molecules and determine which one is the stronger nucleophile

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Q: And which one is the major product?

A: To explain: The major product?

Q: Which of the following is the rule which states that the more substituted product is the major…

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Q: Draw the product of the reaction and propose mechanism of the reaction

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Q: Going down a group, consider the halides: Of the halides shown, which is most basic? Of the halides…

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Q: Draw the main structure of the following reaction

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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: Which is most reactive in electrophilic substitution? Which is least reactant in electrophilic…

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Q: What is the major product of this reaction sequence?

A: Correct option is (b) i.e pentanoicacid acid is the final product.

Q: nucleophile

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Q: Which is the better nucleophile, A or B?

A: This question is related to the topic electrophilicity and nucleophilicity. A nucleophile is species…

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: The reaction of chlorobenzene with acetyl chloride in presence of AlCl3 is a Friedel – Crafts…

Q: Which of the following is most likely an intermediate in the following reaction?

A: As concentrated sulfuric acid is a strong oxidizing agent, it oxidizes some of the alcohol to carbon…

Q: Rxn E кон

A: Cycloalkyl reactant whose elimination and substitution products are to be determined.

Q: In a polar reaction mechanism, the atom that gives away electrons in an uncharged nucleophile will…

A: Given,  In a polar reaction mechanism, the atom that gives away electrons in an uncharged…

Q: What is the appropriate electrophile nucleophile and solvent to achieve this final product

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Q: What is the major following dehydra

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

Q: Draw the other compound in this equilibrium. Why does this product group is in this compound? What…

A: See answer below.

Q: what is the major product of the reaction

A: We have to predict the major product of given reaction.

Q: what are the products of this reaction based on the arrows?

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Q: Drawing the Products of an SN1 Reaction Label the nucleophile and leaving group, and draw the…

A: the nucleophile and leaving group

Q: Elimination reactions require a nucleophile base

A: Elimination reactions  require a nucleophile or base ? The answer and explaintaion of the question…

Q: What

A: We will write the final product of the reaction

Q: is the indicated carbon electrophilic or nucleophilic

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Q: Explain why alkylation of an α-carbon works best if the alkyl halide used in the reaction is a…

A: The alkylation reaction of an α-carbon depends on the R-X (alkyl halide) used in the reaction. The…

Q: What is the final product (D) of the following reaction sequence?

A: In the first step, p-chloronitrobenzene reacts with Fe/HCl followed by NaOH to form p-chloroaniline

Q: Which is the better nucleophile

A: Organic reagents can be divided into two categories electrophile and nucleophile on the basis of the…

Q: Which nucleophile gives the highest overall reaction rate

A: Substitution reactions in which one nucleophile is replaced with another nucleophilei called "…

Q: Choose all the nucleophiles.

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Q: Which of the following is most likely to act as a base rather than a nucleophile?

A: From the given alkoxide most like base is tertiary-butoxide Because it contains more alkyl and it…

Q: Acetal product formation requires an acid catalyst in the second step, but NOT in the first step.…

A: We have to predict whether given Statement is true or not.

Q: What is the product of this reaction Sequence?

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Q: What is the conjugated base of this equation?

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Q: what is the product of the following reaction sequences

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Q: Draw the major organic product formed in the reaction.

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Q: Which out of the given nucleophiles will open the following epoxide at the A carbon? Which will…

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Q: Choose the two major products of the following reaction.

A: The given reactant i.e. 2-bromopentane is a secondary alkyl halide and the reaction is carried out…

Q: which

A: We will write the mechanism

Q: What is the strongest nucleophile, NH3, CH4, CH3O-, or H2O?

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Q: Place in order of increasing nucleophile, and explain

A: Nucleophilicity is closely related to basicity. That means the species which is more capable of…

Q: Identify the nucleophile and electrophile in the given reaction. Show the electron rich and the…

A: Nucleophile is electron rich species whereas Electrophile is electron deficient species

Q: What is the leaving group in the following reaction?

A: A leaving group is a moelcular fragment that departs with a pair of electrons in heterolytic bond…

Q: what is the major product of this reaction

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Q: This reaction is an example of conjugate addition of a nucleophile to an a,ß-unsaturated carbonyl.…

A: The alpha hydrogen to the carbonyl group is acidic in nature and this hydrogen is removed in…

Q: the product of the following reaction.

A: An organic reaction takes place when higher electron density site attacks at the electrophilic…

Q: For the following reaction step, indicate which pattern of arrow pushing it represents. A…

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Q: the principal product of the following reaction

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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: the major product of the following reaction.

A: For the oxidation of tertiary alcohols by KMnO4 , there is a necessity to have alpha hydrogen atoms.…

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.