4. Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed) that synthesize the indicated carboxylic acids. + CHCI3 он + он он Br он + NH HO.

Q: Provide the reagents for the reaction to get the product

A: The given chemical reaction is, The name of the reactant is benzoic acid which is a carboxylic…

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Q: DMSO 0

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Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

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Q: 3. Write in the product of 3-isobutyl-1-heptyne with the following reagents: 1. ВНз 2. Н,Ог, "ОН 1)…

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Q: What type of synthesis is this an example of?  Is this showing the addition of a ketone giving a…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: How would you synthesize the following compounds from butanoic acid using reagents from the table?…

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Q: Show the product formed as a result of the reaction between propanoic acid and benzylalcohol in an…

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Q: -! Starting from ethane, outline a method of synthesis of meso 3,4 dibromohexane. SHOW ALL THE STEPS…

A: At first ethane is treated with one mole Cl2 under photolytic condition to get ethyl chloride. Two…

Q: 1. For the reaction scheme below: NH,Et Et Me (i) Give the structure of the product and provide…

A: The answer is given as follows

Q: 2. Reactivity of Carboxylic Acid Derivatives a. Rank the following carboxylic acid derivatives in…

A: Nucleophilic acyl substitution reaction are defined as the class of substitution reaction that…

Q: Propose a plausible curved arrow mechanism for the following transformation: HN-NH2 NH pyridine NH

A: This is a carbonyl substitution reaction type

Q: Complete the following syntheses by providing the reagents and conditions at the reaction arrows.…

A: 1.  Friedl craft's alkylation : alkylation of benzene, -Br group is ortho/para directing group…

Q: 1. Н,о, кон 2. Н-О, НC он HO. p-cresol chloroacetic acid p-methylphenoxyacetic acid

A: A precipitate is formed when a solution consisting of a specific cation is mixed with an additional…

Q: Show the product formed as a result of the reaction between propanoic acid and benzyl alcohol in an…

A: The structure of propanoic acid is; The structure of benzyl alcohol is;

Q: Starting with 3,5-hexadiyn-1-ol, select reagents from the table below that should be used to…

A: The reagents are faigb i) protection with TBDMS-Cl ii) deprotonation of terminal alkynes iii)…

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A: Since you have posted multiple questions as per guidelines we will solve only the first one for you.…

Q: how would you deconstructing” a target molecule into its readily available, simple starting…

A: This synthesis involves Michael addition, aldol condensation, hydrolysis and decarboxylation

Q: 4. For the reaction provided below, give strutures of product C and by-product D. If dimethylamine…

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A: LiAlH4 is a reducing agent which reduces acid to alcohol.

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: This is an example of Diels-Alder reaction followed by cyclization and aromatization.

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A: The major form of given diol-aldehyde exist can be drawn as

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A: Reaction of butanal with sodium borohydride is the reductuion of butanal to butanol.  Reaction with…

Q: sayura OH H + CH ₂ OH ? ?

A: Esterification - it is the process in which carboxylic acid react with alcohol in the presence of…

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A: 2. a. We have to tell why the reaction in the scheme (1) is easily done under mild conditions and…

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A: In a SN2 reaction a nucleophile attack the leaving group contaning Carbon and remove leaving group…

Q: 4. Provide a detailed, stepwise mechanism for the reaction below. (CH3)2CHCH2CH2CH21 + CN- →…

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Q: The following synthesis requires more than one step. Specify the reagents you would use to carry it…

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Q: 2. Draw out the forward synthesis (fill in the boxes) only for the following transformation (it'll…

A: Here we have to make a desired forward synthesis for below conversion .

Q: 2. For the following amines A and B, show all of the Hoffman elimination produc If one product is…

A: The Hofmann Elimination is an elimination reaction of alkylammonium salts that forms C-C double…

Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

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Q: Give a brief answer to explain why acetic acid has a much higher BP (118 C) than 1- propanol (BP =…

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Q: QUESTION Complete the following synthetic transformation by selecung from the list of reagents below…

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Q: В. i. Draw the possible conformations for trans-1,4-dibromocyclohexane. Show the most stable…

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Q: 2. Which compounds would you heat together in order to synthesize the following?

A: Diels-Alder reaction: The Diels–Alder reaction is a pericyclic reaction (cycloaddition) between a…

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Q: Q2Show why the OH functional group, of phenol below, is ortho directing using curly arrows to show…

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