Oxidation reactions can be used in multistep syntheses to produce new functionalities for use in subsequent reactions. Consider the following multistep reaction when you draw the structures in Parts 1 and 2 below. Please explain mechausms fove the products I and 2 но HO PCC I. NaH Product I Product 2 Br CH,CI, Step 1 Step 2

Q: H2 Lindlar's catalyst H2 Pd/C NaOEt O १/ Br

A: Product of following reaction can be made by applying appropriate reaction mechanism.

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

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: Propose an efficient synthesis for the following transformation: The transformation above can be…

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Q: In the first step of the reaction sequence shown, two products are obtained. Each of these products…

A: Given

Q: Please assign the correct letter to each reaction.

A: The name of the alkene given is But-2-ene.

Q: Select the major organic product of this reaction. H3C, H3C_ A OTs OTS но H3C. D NaOH, H2O B -OTS…

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Q: Predict the structure of the product formed from the given reaction. Br 3-Bromocyclohexanol O Br Br…

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Q: H H 19. Provide the major organic product in the reaction below. H3C H CH 3 CH 3 1. BH3/THF 2. NaOH,…

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Q: Predict the major products of the given reaction. a NH + NH₂ NaOH + og O og8m². Na O OH + + + ³m². 8…

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Q: Predict the product(s) OR reactants for the reactions by drawing the appropriate structure(s) in the…

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Q: Provide the product of the following reaction, by writing the nume O Br HOCH₂CH₂OH H₂SO4 Mg.

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Q: The following synthesis could be used to generate a compound used as a spice in Dr. Erb’s tacos.…

A: Ans only ii

Q: НО. ОН H+

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Q: What is(are) the major organic product(s) of the reaction shown below? NaCN H3C CD3 С. ÇN H А. В.…

A: Ring opening reactions of epoxide

Q: 1. NaH Me ENO I Me 2. A 1. xs Mel 2. Аg:0, H,0, 4 В 1. NaNg 2. LIAIH, 3. aqueous workup H3O", A но.…

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Q: What is the best reagent to use for the following reaction? ii O NaBH4, methanol O 1. LiAlH42. H30+…

A: Other answer choices listed in the image are also potential reducing agents, but they might not be…

Q: NEt HO. HNE + Br NH, (a) (b) (c) (d) proparcaine EIOH, H* (a) NaOH, Ф), HNO,, H,SO, (1), H* H2. Pt…

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Q: What is the major product of the following reactions? HO SH SH o1. он 02. SH 03. он 04. o5.

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Q: Give the structure of the product from Step 2. Be sure to include all lone pair electrons and formal…

A: 1. PCC: Pyridinium chlorochromate: It is a mild oxidizing agent.This is used to oxidise primary…

Q: Can you show the steps to achieve the products and the mechanism? And can you see if the product is…

A: The addition of BH3 occurs in a such way that the hydrogen atom adds to more substituted carbon and…

Q: What is the major product to the following reaction? H20 H2SO4

A: Please find your solution below :

Q: 4. In the following reaction, write the possible product(s) formed under the following conditions,…

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Q: Select the correct product of the following reaction series. EtO NHAC OEt 1. NaOEt, EtOH 2. Br 3.…

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Q: Which of the following reactions form the product shown. NaOH Cla H-O H20 CH 1.(CHCOH, Hg(0-CCF2 2.…

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Q: Additional Questions: Use the reactions in this packet as well as others you have learned. 1.…

A: LiAlH4 is strong reducing agent reduces all functional groups. It is non selective reducing agent.

Q: Identify reagents that can be used to achieve the following transformation: OH O 1) NaOH, 2) RCO3H,…

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Q: Complete the following synthetic transformation by selecting from the list of reagents below. Each…

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Q: H3CC=CH₂ Br Mg ether A H₂O B

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Q: H a. Ho b. C. 1) NaOH, Cl₂ 2) H3O*, A 1) NaOCH3 2) H+, A 1) NaOH 2) H₂SO4, A

A: The given reactions are shown below.We have to provide the major product of the given reaction.

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.