a. к -ОС(СH)3 Br C. [1] CH,I (excess) [2] Ag20 [3] A NH2 b. к -оС(CH)з CI d. [1] CH,I (excess) [2] Ag,0 [3] A `NH2

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Sn/HCI Drawing NO2 Pro Atom…

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Q: Draw a stepwise mechanism for each reaction.

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Q: Draw the product formed when each organometallic reagent is treated with H2O.

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Q: Label each substituent as an ortho, Para, or meta director. COOCH3 NHCOCH3 CH3

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Q: Match the correct reagents with each step A B

A: The starting reactant is an terminal alkyne to which a methyl, -CH3 group is added with the help of…

Q: 4. Draw the ketone tautomer of each enol present under slightly acidic conditions. H

A: Keto–enol tautomerism is a chemical equilibrium between a keto form (a ketone or an aldehyde) and an…

Q: 1) CH3CI, AICI 2) 3 mol NBS ? Modify the given copy of the starting material to draw the product.

A: Friedel-Craft alkylation reaction: When the benzene reacts with an alkyl halide in presence of Lewis…

Q: Br. Br NaOCH3 DMF

A: SN2 reactionIt is a bimolecular nucleophilic substitution reaction in which the rate of reaction is…

Q: Classify each carbocation as 1°, 2°, or 3°. b. (CHa),CCH2 a. С. d.

A: NOTE: Since you've posted multiple sub-parts, we'll solve only the first three sub-parts for you. To…

Q: Circle all molecules that contain acetals.

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Q: Draw a stepwise mechanism for each reaction.

A: (a)Given reaction is shown below:

Q: OMe OMe H2SO4 2 equiv. OMe OMe

A: Given reaction is : Draw an arrow pushing mechanism and explain why less than two substitutions are…

Q: Draw 3-methylcyclohex-2-enone

A: Given Chemical Name = 3-methylcyclohex-2-enone Structure = To be determined

Q: mela H3C CH3 H₂C CH3 NaSCH 3 NaOCH3 O SCH3 CH3 H3C OOCH3 CH3 H3C

A: The question is based on the concept of nucleophilic addition reactions. We need to identify the…

Q: f. g. h. a a a= 6 = Xe Br2 CH3CH₂OH H₂SO4 H₂ Pd/C

A: The given reaction is an example of anti- addition reaction of bromine on olefins . In this type of…

Q: 2) Draw all products formed in the following SN1 reaction. Br CH;CH2OH

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Q: Draw the major product of the following reaction. H2 5-methyl-2-hexyne Lindlar's catalyst

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Q: HBr Draw Alcohol Product Draw Alkyl Halide Product 1

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Q: Draw the major monochlorination product of this reaction.

A: Given is organic reaction. The given starting compound is alkane.The given reaction is photochemical…

Q: Draw the structure of the organic product of the following transformation. cat. ACOH `NH

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Q: Draw the more stable enol for each structure. hoo000.000

A: the solution is as follows:

Q: О-Н a) CH CH C CHCH ynsb d mwodt noo edi nomoai3 ol fobuboig ad to mo ldieog ls ors wsi0 (d ds adt…

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Q: Draw the major organic product of this reaction after workup. Draw the product that contains the…

A: The objective of the question is to identify the product.

Reactive Intermediates

In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.

Hydride Shift

A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.

Vinylic Carbocation

A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.

Cycloheptatrienyl Cation

It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.

Stability of Vinyl Carbocation

Carbocations are positively charged carbon atoms.  It is also known as a carbonium ion.