Q: 1. Which are the starting materials used to synthesize the given compound through reductive…
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Q: 6. The reaction between aniline and nitrous acid at low temperature yields A) an N-nitroso amine B)…
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Q: 2) Compound B (C,H30) is a carbonyl compound that give negative result on Schiff's test. CompoundB…
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Q: 5. The following aminoketone can undergo an intramolecular reductive amination. Draw the expected…
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Q: N-Nitroso amines are stabilized by electron delocalization. Write the two most stable resonance…
A: Resonance is the delocalization of electrons to via double bonds.
Q: Draw the products formed when each attached amine is treated with [1] CH3I(excess); [2] Ag2O; [3] Δ.…
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Q: Show how you would convert propan-1-ol to the following compounds using tosylateintermediates. You…
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Q: 2) Predict the products formed when the following amides are treated with bromine and sodium…
A: Hoffman reaction
Q: 9. What is the major Hofmann elimination product formed from the following amine? CH3 CHs. NH2…
A: Explain : Hoffmann elimination Reaction : Hofmann elimination is an elimination…
Q: 2) What amine can be used to produce the following imine from a ketone or aldehyde? NH2 А. В. `NH2…
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Q: Chlorpropamidé håš a lohger NH NHCH,CH,CH,CH, NH NHCH CH,CH,CH, Tobutamide Chlorpropamide Which of…
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Q: Which of the following is FALSE about the reaction below? +0₂N NH₂ Select one: Oa. It is initiated…
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Q: Question attached
A: Amines on reaction with HCl result in the formation of amine salt. Primary amines give primary amine…
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Q: 3. For the following amines, propose a stepwise synthesis for each compound. ? NH2 a) OH b)
A: Step 1 The given amines can be formed using the alkenes as one of the reactants and with the use of…
Q: 3. Carbonyl (C=O)-Containing Compounds (5) a. b. С. d. е.
A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…
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Q: t)which B the fallowing Statements is true regardirg N- phenylocetamide ? 5aka a cetanilide Lamide…
A: This question is related to general organic chemistry. N-phenyl acetamide has an amide functional…
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A: The first step involved in the reaction between amine and carboxylic acid is given below
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Q: Benzenesulfonyl chloride or p-toluenesulfonylchloride give N-substituted sulfonamides with primary…
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Q: 1. Which is more reactive? a. carboxylic acid b. acid anhydride c. acid halide d. amides e. esters…
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Q: Which of the following reducing agents is used in a reductive amination? You may choose more than…
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A: Aldehyde and ketone in presence of an acid reacts with secondary amines to give enamine . So the…
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A: Alkyl azide have general formula R-N3
Q: What results when dimethylsulfide is treated with methyl iodide? 1) CH,I 2)- NH 3) -H A. B. C. D.
A: The reaction taking place is given as,
Q: 5. show two different ways of preparing each of the following compounds via a reductive amination:…
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A: a) Reductive amination is a two-venture strategy that changes over aldehydes and ketones into…
Q: CH, NH 1. Excess CH;I 2. Ag,0, H,O, heat
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Q: What products are obtained when the following tertiary amines react with hydrogen peroxide followed…
A: The tertiary amines have three alkyl groups attached to a nitrogen atom. They undergo various…
Q: Which amide would you treat with LIAIH4 to prepare the following compound? CH2NHCH3 CH2-C-NH2…
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Q: Rank the following compounds in order of increasing basicity and explain the order you chose.
A: Lone pairs are present in the pyrrole molecule and these lone pairs are in conjugation with the…
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A: The true statement regarding aliphatic amines has to be given,
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Q: Show how you would use appropriate acyl chlorides and amines to synthesize thefollowing amides.(a)…
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Q: Rank the following compounds in order of increasing basicity: I. p-nitroaniline…
A: The basicity of a compound is the tendency of the atom to donate its lone pair. More the electron…
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A: Reductive amination of aldehyde A with amine B changes the aldehyde group to amine. The most basic N…
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A: Structure of N-methylethanamine is as follows. N-methylethanamine is a secondary amine. Structure…
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Q: H. А В C
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Q: 2) Use compound C (shown below) to answer the following questions. H2N CH, H compound C H3C Br a)…
A: 2. A. Secondary amine B. (2R,3R)-2-amine-3-bromo butane C. Compound A &C is enantiomers…
Q: a) What are the difficulties with the following reaction to synthesize an amine. + HBr Br + NH NH2…
A: Given reaction is :
Q: Rank the following compounds in order of increasing basicity and explain the order you chose.
A: The resonance structures of pyrrole are shown below. The above structures imply that lone pair of…
Q: 3. For the following amines, propose a stepwise synthesis for each compound. ? NH2 a) ÓH ? b) ZI
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Q: Which of the following reaction or reagent does not produce an amine molecule? A. Curtius…
A: The given reactions are A. Curtius rearrangement B. Reaction of oximes with metallic sodium in…
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A: Given: Synthesis of (+/-)-amphetamine from 1-phenylpropan-2-one
Q: (a) Explain why phentermine [PhCH2C(CH3)2NH2] can’t be made by a reductive amination reaction.(b)…
A: (a)The structure of phentermine is given below.
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- Is the acid-catalyzed hydrolysis of acetamide a reversible or an irreversible reaction? Explain.Several compounds have been found to inhibit -lactamase, and drugs based on these compounds can be taken in combination with penicillins and cephalosporins to restore their effectiveness when resistance is known to be a problem. The commonly prescribed formulation called Augmentin is a combination of the -lactamase inhibitor shown below with amoxicillin (shown above). It is used to treat childhood ear infections when resistance is suspected, and many kids know it as the white liquid that tastes like bananas. Which of the statements below are true statements? 1. The stereochemistry of the fusion between the four-and five-membered rings in the inhibitor and amoxicillin are different. 2. The inhibitor possesses enol ether and allylic alcohol functional groups while the antibiotic possesses a phenol and a secondary amide functional group. 3. Neither the inhibitor nor the antibiotic contains strained rings. 4. Both 1 and 2 are true.What aldehyde or ketone and nitrogen component are needed to synthesize N-ethylcyclohexanamine by a reductive amination reaction?
- Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only aldehydes to aminesDraw the products formed when each attached amine is treated with [1] CH3I(excess); [2] Ag2O; [3] Δ. Indicate the major product when a mixtureresults.Show how you would use appropriate acyl chlorides and amines to synthesize thefollowing amides.(a) N,N-dimethylacetamide (b) acetanilide (PhNHCOCH3)
- Show how to synthesize the following amines from the indicated starting materials byreductive amination. (±)-amphetamine 1-phenylpropan-2-oneThe pathway for nicotinic acid requires a series of highly unfavorable reactions. Which other alkaloid molecular scaffold would you use to arrive to such a molecule? And, which series of hypothetical enzymes would you use?N-Nitroso amines are stabilized by electron delocalization. Write the two most stable resonance contributors of N-nitrosodimethylamine, (CH3)2NNO.