CF3 „CF3 CH3NH2 н (S)-fluoxetine

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A: A step wise mechanism is as follows

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Q: Form the B to C by reagent and reaction missing! (ONLY USE ALKYLATION NOT

A: The answer is as follows:

Q: What reagents are needed to carry out the conversion shown? HO i ㄷ O HOCH₂CH₂OH, H₂SO4; CH3CH2AICI3…

A:

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Q: H₂N

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A: (a)  The poly(vinyl alcohol) cannot be prepared by the radical polymerization of vinyl alcohol…

Q: (c) ECH H₂ Pd/C (d) CH₂C=CCH₂CH3 + D₂ Draw the product of reaction (c). Incorrect Lindlar catalyst…

A: Alkynes can undergo reduction to form either alkenes or alkanes, depending on the specific reagents…

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A:

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A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: (13) A B C OD What is not an elementary step in the mechanism for the following reaction? H₂O НО. X…

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A: Given compound:

Q: 2. Propose a mechanism to explain the following reaction. ОН om a + CH3 H₂SO4 Aer heat CH3 CH3

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A: SOLUTION: Step 1: The acetylene molecule is deprotonated in the presence of NaNH2 and then alkylated…

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A: Structure of Given molecule:

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A: 1- First we will see tha Products for each by using ring closing metathesis.

Q: Fluoxetine synthesis from Michael Addition reaction

A:

Q: Problem 21.20 Give structural formulas for the reagents, intermediates, and products symbolized by…

A: Answer:

Q: Provide an IUPAC name for the structure shown.

A: This question is based on IUPAC nomenclature of an organic compound.

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A: Given compound:

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A: The overall reaction for the entire synthesis with the catalyst are given below:

Q: AICI,

A: Using concept of fredalcraft acylation ,this can be determined.

Q: None

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Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.