Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement.  Which bond moves in the carbocation rearrangement?  Which compound shown below has that appropriate bond in pink?

Q: Draw the starting alkyne that would lead to this major product under these conditions.

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Q: Choose all the nucleophiles OH-     H3O+     NH4+     CH3OH     (CH3)3CLi     CH3CH2CH3     NaNH2…

A: Nucleophile :-A chemical species which have free pair of electronsor can denote pair of electrons…

Q: Identify the cyclohexyl substrate which would undergo the fastest E2 with base.

A: E2 elimination is a one step concerted mechanism reaction in which dehydrohalogenation (or any other…

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: Draw a complete stepwise arrow-pushing mechanism the correctly predicts the major product of the…

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Q: What is the reagents/conditions to perform the following transformation? Problem viewing the image,…

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Q: The reaction shown here yields three different nucleophilic substitution products that are…

A: Nucleophilic Substitution reaction- The replacement one atom or group of atom from reactant…

Q: detailed electron pushing mechanism fkr this reaction. It needs to be done as an SN2 reaction.…

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Q: Draw the major product(s) of the following reaction

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Q: Draw all products, including stereoisomers, in the following reaction.

A: The given reactant is a 3° (tertiary) alkyl halide.

Q: major product.

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Q: The following reaction is done with a low concentration. What type of substitution mechanism will be…

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Q: What hypothesis did the Hammond Postulate help us to craft regarding the stability of carbocations…

A: according to hammond postulates. the transition state resembles to either reactant or product which…

Q: Please draw the major product/products of each of the following reaction

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Q: Make one reaction scheme using proper compounds in the box below for Williamson ether synthesis.…

A: The reaction given is Williamson ether synthesis.

Q: Image attached

A: Alkyl halides on reaction with strong base undergo elimination reaction. In product double bond…

Q: Draw the major organic SN1 product for the reaction shown.

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Q: Draw a mechanism for the reaction of the ketone with hydronium ion. In the first box, draw any…

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Q: hoose the compound below that gives a carbocation intermediate that undergoes rearrangement?

A: D will undergoes the rearrangement in intermediate of carbocation.

Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

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Q: Which nucleophiles will add to the following conjugated enone at the A carbon?  Which will add at…

A: The compound given is,

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

A: the nucleophile and leaving group

Q: Consider the nucleophilic substitution reaction shown here. Based on the stereochemistry, does it…

A: Nucleophilic substitution reaction is the kind of reaction where electron-rich nucleophile attacks…

Q: Major product and mechanism for this reaction?

A: The details solution for this reaction is provided below in attach image.

Q: The following four reactions will be the focus of the upcoming chapters (substitution and…

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Q: For each of the following pairs of substrates, which do you think will undergo an Sn1 reaction…

A: SN1 reaction is a nucleophilic substitution reaction . This reaction involves formation of a…

Q: Propionaldehyde undergoes an aldol condensation to form the aldol dehydration product. HCI = Product…

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Q: Choose the major product of the following reaction sequence

A: The details solution for this reactions is provided below in attach image.

Q: Draw the MAJOR product(s) of the following reaction.

A: Additon of water :  Alkene by addition of water in presence of  Hg(OAC)2 gives alcohol is the…

Q: is this an E1 or E2 mechanism for this reaction? What is the major product and mechanism for it?

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Q: e major product of

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Q: monobromination

A: Br2 give Radical substitution reaction in the presence of sunlight. Inwhich Br2 broken in Br•…

Q: Draw the major product(s) of the following reaction.

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Q: Draw all product(s), mark them as major and minor. If stereochemistry at any site is important, be…

A: Substrate- secondary sulfonic ester Reagent (NaSH) - Strong nucleophile Solvent (DMSO) - Polar…

Q: Draw the major product of each of the following reactions.

A: Alkenes reacts with Br2 and undergo addition reaction producing dibromo alkane. The addition…

Q: Which of the following statement(s) is (are) TRUE? a. Zaitsev's rule: If substrate is a tertiary…

A: Zaitsev rule is concerned with the the possible elimination products in an organic reaction. The…

Q: Which reagent(s) will result in the nucleophile attacking the more substituted side of an epoxide?…

A: The question is based on the concept of organic reactions. It involves ring opening  of the epoxide…

Q: Draw

A: Missing reagent should be nucleophile which attack on carbonyl carbon.

Q: Draw a curly arrow mechanism to clearly describe why the following reaction gives a trans dibromo…

A: Reaction of alkenes with bromine results in the formation of vicinal dibromides i.e. 1,2-dibromides.…

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: Draw the reaction mechanism of this reaction and state whether it is a SN1 or SN2 reaction.

A: We have to predict mechanism and type of reaction.

Q: CI CH3CH20H

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Q: terminal alkene

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Q: What is the most likely product from the following sequence

A: The first step of the reaction is the Friedel-Kraft acylation reaction and the second step of the…

Q: Draw the major 1,2-addition product and the major 1,4-addition product of the following reaction.…

A: The thermodynamic product is formed at higher temperature.

Q: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

Q: Draw both resonance structures of the most stable carbonation intermediate in the reaction shown…

A: No alpha hydrogen increases the stability of carbocation increases.

Q: Draw a complete, step-wise, curved arrow mechanism for each reaction shown below. You don't need to…

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Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.