Draw the major organic product of the reaction shown.

Q: Draw the structure of the intermediate that leads to the major product in the following reaction. Be…

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Q: Draw the detailed mechanism and the product for the following reaction. Be sure to include…

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Q: Select one activator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Here, I take -OMe (methoxy) group as an activator.  In case of anisole, the l.p. present on -OMe…

Q: TH.

A: Given images are : Increasing order of rate of nucleophilic addition = ?

Q: Br H-Br

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Q: Bonus Question: If you deemed the previous reaction to be unsuccessfull, propose a reaction or…

A: To get the starting molecule we will do the retrosynthetic analysis and by doing this we get toluene…

Q: The mechanism for this reaction is the reverse of the one in Eg. 18-13. H3CO OCH3 Hао (ехсess) + 2…

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Q: (SYN) Show how to make each compound from an alkene. (a) (b) OH HO

A: There is 2 process of alcohol formation from alkene Hydration of alkene forms a carbocation…

Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. cat. H2SO4 HNO3 (1 equiv)

A: Nitration of aromatic compound: Aromatic compound reacts with the nitrating mixture to form a…

Q: NBS

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Q: Synthesis this please. Include reagents that could work and intermediate compound. N

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction can be drawn as

Q: Draw the carbocation intermediate of the reaction and arrows showing the resonance.

A: See the images belowExplanation:

Q: Bonus: What anion is a more reactive nucleophile? Why? Must draw a picture! VS.

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Q: Step 1 Step 2 Step 3 Step 4 i Draw H3CH2C¯, and then add the curved arrow notation showing a…

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: b. Br EtO/EtOH

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Provide a multi-step synthesis of the target structure on the right from the starting structure on…

A: Here we are required to synthesize the given compound from given alkane

Q: Draw the complete, detailed mechanism for the reaction: conc HCI ?

A: In rection of alkene , at first,  alkene donate electron to H+  and carbocation intermediate is…

Q: Draw the product of the following reaction. HNO: H;SO,

A: The given reaction is Nitration. In this reaction one of the hydrogen atom is replaced by nitro…

Q: Draw the complete, detailed mechanism for the following reaction. 1. ¸MgBr 2. H3O+ (excess)

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: The attached reaction does not afford the major product that is given.Explain why this is so, and…

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Q: D July 애 H Drodunt

A: Debromination gives primary carbocation. Now, elimination of proton gives product.

Q: + HO Br

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

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Q: For each of the following pair of species, which is the stronger nucleophile in acetone? Explain.

A: Given : structure of molecules Tip : less electronegative atoms are strong nucleophile

Q: 1. HBr 2. NaCN, DMSO

A: Markovnikov's rule states that when an asymmetrical reagent is added to an asymmetrical alkene, then…

Q: Draw the major monobromination product of this reaction. NBS, light

A: Answer:When substitution reaction takes place through the formation of free radical intermediate…

Q: Please help me with a possible drawn synthesis for the shown reaction. Carbons should come from…

A: Step 1: Step 2: Step 3: Step 4:

Q: 4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism…

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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.