A) ethylmethylpropanamide B) N-ethyl-N-methylpropanamide C) N-ethyl-methylpropanamide D) N-methyl-ethylpropanamide E) N,N-ethylmethylpropanamide

Q: 19. What is the IUPAC name of the following amine? N. (a) N-methyl-N-propxlnentanamine (b)…

A:

Q: Amines and Amides 5. Base Hydrolysis a. Acetamide b. Benzamide

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Q: Test for Amines a. Hinsberg test: b. Nitrous acid test:

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Q: How to synthesize aspirin without using acetic anhydrid

A: Aspirin is known as acetyl salicylic acid.It is used as pain reliever for fever,body ache etc. Here…

Q: Why can you not use this reaction to make a secondary amine? a) Alkyl halides are weak…

A: Since in the above reaction, the secondary amine formed will have more inductive effect compared to…

Q: Draw the following  a) N-methylpropanamideb) cis-2-heptenec) 2-hexanone d) butylbutanoatee)…

A: Step 1: Step 2: Step 3: Step 4:

Q: 17.56 What amides will form each amine on treatment with LIAIH4? a. oso b.

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Q: Order the compound according to increasing boiling point: a) 3-pentanone b)2-methylcyclopentene…

A: Boiling point depends on the intermolecular forces acting between the molecules. The more are these…

Q: The following three derivatives of succinimide are anticonvulsants and have found use in the…

A:

Q: Hinsberg's Method to determine, 1°, 2°, 3° amines. Draw the structure of the products of the…

A: Given,

Q: Select one: A. It has an antioxidant effect. OB. It shows an antiviral effect OC. It can undergo…

A: Organic Compound: The type of chemical species which can be extracted by living organism /labotrical…

Q: КОН HEN H.

A: B) The reactant given is an amide. Hence it will react with base KOH and undergo hydrolysis reaction…

Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium salt when it reacts with…

A:

Q: Why we used the phenolphthalein

A: Phenolphthalein is an acid-base indicator used for detection of end point of titration of acid and…

Q: 21.1 Draw the structure. N-methylpropanamide

A:

Q: Using functional groups, determine why DEET (N,N-diethyl-meta-toluamide): a) is insoluble in water…

A: The given compound contains toluene, tertiary amide and two ethyl groups. The name of the compound…

Q: what is the product of a reaction between maleic anhydride and phellandrene?

A: The product of reaction between maleic anhydride and phellandrene is shown in step 2.

Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium ion when it reacts with…

A: To understand the reaction consider the reaction of a primary amine with nitrosonium ion. The…

Q: A drug can exert its pharmacological effect only if it is

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Q: What is a correct name of the following compound ? NH O acetanilide O methylacetanilide…

A: The given compound is an amide (RCONH2) as it has a carbonyl group directly attached to N atom.

Q: If 2-pentanone and diethylamine underwent a reductive amination, what would be the major product? O…

A: Reductive amination reaction involves the formation of C–N bond from secondary amine and a carbonyl…

Q: Show how to convert amines to other functional groups, and devise multistepsyntheses using amines as…

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Q: Which of the following is a secondary amide?

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Q: 8) When pyridine is treated with a mixture of nitric and sulfuric acids, the major EAS product is:…

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Q: Draw the major product formed by treating each amine with excess CH3I, followed by Ag2O, and then…

A: The general reaction involved in synthesis of alkenes from amines is recognized as "Hoffman…

Q: I need help my unknown is an amine after doing a solubility test so I performed the Hinsburg test…

A: Step 1: Step 2: Step 3: Step 4:

Q: A H₂N BHN NH C. NH₂ COOH Arginine O A, B - heterocyclic aromatic amines, C - 1º aliphatic amine OA -…

A: Given compound:To determine:Types of Amine

Q: Draw the following a) N-methylpropanamide b) cis-2-heptene c) 2-hexanone d) butylbutanoate e)…

A:

Q: 1. Circle the structure corres a) 3-chlorobenzoic acid CI b) Methyl propionate H3CH₂C H3C H3C d)…

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Q: MC 10 How many equivalents of LiAIH4 do the following molecules require for their conversion to…

A: LiAlH4  is Lithium aluminium hydride which is a good reducing agent, and can convert aldehydes to…

Q: b) Fill in the boxes to synthesize the following primary amines i) ii) iii) iv) Br NH O 1) 2) 3)…

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Q: What identification tests can be performed to determine isoamyl acetate?

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Q: Isomer of N-Butyl-N-Ethyl-Hexenamide   A.) Dodecanamide       B.) N,N-Dibutyl-butanamide       C.)…

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Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium ion when it reacts with a…

A: Given reaction is:

Q: Give each of the following amines an IUPAC name.

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Q: What starting materials are needed to prepare each drug using reductive amination? Give all possible…

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Q: 32 which can be used to prepare amine usmg Gabriel Jynthesis? seict all that apply…

A: The following compound can be used to prepare amine in Grabiel synthesis.

Q: N. carbonyl compound amine Select one: NH2 a. „NH2 O b. HN O d. + ZI

A: When a ketone or Aldehyde (carbonyl group containing Compound) is treated with amine , then imine is…

Q: 4-B Question) Draw the following by Chemdraw? 1 Acetamides 2 Benzamides 3 Benzenesulfonamides 4…

A: This question belong to IUPAC Nomenclature of organic compounds. I have draw all part with the help…

Q: Draw the following  a) N-methylpropanamide b) cis-2-heptene c) 2-hexanone

A: “Since you have posted a question with multiple sub-parts, we will provide the solution only to the…

Q: 22. The stability of carbocation can be accounted by which of the following structural effect? a.…

A: Please find your solution below : 22. The stability of carbocation can be accounted by both…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.