Q: What 1° amine and carbonyl compound are needed to prepare each imine?
A: a. The given compound is, 1° amine and carbonyl compound are needed to prepare the above compound…
Q: 2) Propose two ways to synthesize the amine shown starting with an alkyl halide. (3
A: The reactions involving organic compound are known as organic reactions. Amines are organic…
Q: Draw the major product formed from Hofmann elimination of the following amine. CH3 [1] CH3I (excess)…
A: Hofmann elimination: Elimination of group to form alkene is known as hofmann elimination. Only…
Q: 5. The following aminoketone can undergo an intramolecular reductive amination. Draw the expected…
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Q: Draw the products formed when each amine is treated with [1] CH3I (excess); [2] Ag:0; [3] A.…
A: Hofmann elimination is a reaction in which amines are eliminated from the molecule to form alkenes.…
Q: II. Draw the structures of the ff: A. N-ethyl-N-phenylpropanamide B. 3-hydoxy-N-methyhexanamide C.…
A:
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: 2. What is the structure of the amine that on reaction with the acid chlorides , will give a…
A:
Q: Draw the products formed when each attached amine is treated with [1] CH3I(excess); [2] Ag2O; [3] Δ.…
A: In the given question we have to do the stepwise Reaction. 1,2-dimethylcyclopentanamine reacts with…
Q: What products are formed by hydrolysis of each imine or enamine?
A: The products are formed by hydrolysis of each imine or enamine has to be determined.
Q: 1.answer the following questions A. What is reagent used to convert secondary amine to tertiary…
A: A. Secondary and Tertiary amines are those in which N atoms are bonded with two and three alkyl…
Q: Show how you would convert propan-1-ol to the following compounds using tosylateintermediates. You…
A: One of the methods of amination of an alcohol involves the conversion of an alcohol to the tosylate…
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: 6. Draw the products formed upon Hofmann Elimination of the two isomeric amines below. (Excess CH3-I…
A: Detail mechanistic pathway is given below
Q: 2) What amine can be used to produce the following imine from a ketone or aldehyde? NH2 А. В. `NH2…
A:
Q: Chlorpropamidé håš a lohger NH NHCH,CH,CH,CH, NH NHCH CH,CH,CH, Tobutamide Chlorpropamide Which of…
A: Tolbutamide is a first potassium channel blocker, sulfonylurea oral hypoglycemic medication. When…
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: 2 Draw structures to correspond with the following common and systematic names:(a) phenyl formate…
A: a).The given compound is phenyl formate. The molecular formula of phenyl formate is C7O2H6. The…
Q: Write the complete stepwise mechanism for the acid-catalyzed hydrolysis of the following amide to…
A:
Q: Which amide would you treat with LIAIH4 to prepare the following compound? -CH2NHCH3 -CH2-Ċ-NH2…
A: Amides are reduced to amine on reaction with lithium aluminium hydride to give the corresponding…
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…
Q: - How might the following amine be prepared using reductive amination reactions? Show all precursors…
A:
Q: Draw the two starting materials from which the following product can be made from the reductive…
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Q: Which of the following reducing agents is used in a reductive amination? You may choose more than…
A: An organic conversion is a process of converting one organic chemical to another organic compound…
Q: - How would you prepare the following amines, using both Hofmann and Curtius rearrangements on a…
A: The Hofmann and Curtius rearrangement involves the conversion of carboxylic acid to an amine. The…
Q: Friedel-Crafts reactions take place when amines are acetylated. Select the correct response: O True…
A: Friedel crafts alkylation or acylation is reaction of alkyl halide with benzene in presence of lewis…
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:…
A: In reductive amination reaction, carbonyl compound reacts with ammonia or amine to form an imine…
Q: What starting materials are needed to prepare each drug using reductive amination? Give all possible…
A: Reductive amination involves the formation of a primary, secondary or tertiary amine by the reaction…
Q: Explain why imidazolides are much more reactive than other amides in nucleophilic acyl substitution.
A: It is known that, imidazolides are much more reactive than other amides in nucleophilic acyl…
Q: H2N NOBH3 (N, DCE
A: Detail mechanistic pathway is given below
Q: 3. If the compound shown is subjected to reaction conditions that will hydrolyze amides one of two…
A: Solution of the question is given below:
Q: Which amide would you treat with LIAIH4 to prepare the following compound? CH2NHCH3 CH2-C-NH2…
A:
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…
Q: What starting materials are needed to prepare each drug using reductive amination? Give all possible…
A: Reductive amination involves the formation of a primary, secondary or tertiary amine by the reaction…
Q: What is the product of the following reductive amination? CH, CH, NHz mild acd Nafity or Na BH3CN…
A: This is an typical example of reductive amination. The details solution for this reaction is…
Q: What are the products of reactions of aldhydes and ketones with (I) chloroform (ii) primary amines?
A:
Q: 10.₁ amide? A. one equivalent B. two equivalents C. this conversion is not possible D. one…
A: Following questions are belongs to the reaction mechanism.
Q: Draw the product of attached reductive amination reaction.
A: The product of the given reductive amination reaction has to be given.
Q: Which amines cannot be prepared by the Gabriel synthesis? Explain your choices
A: The Gabriel Synthesis of primary amines: The Gabriel Synthesis consists of two steps and uses a…
Q: Which of these amine will react fastest in a reductive amination reaction?
A: Reductive amination is the successive conversion of primary amine into secondary amine and tertiary…
Q: 1. State all the products formed from Hofmann elimination of the following amine. Choose the major…
A: Hofmann's elimination : Hofmann's elimination is the process of creating tertiary amines and alkenes…
Q: a) What are the difficulties with the following reaction to synthesize an amine. + HBr Br + NH NH2…
A: Given reaction is :
Q: 3. For the following amines, propose a stepwise synthesis for each compound. ? NH2 a) ÓH ? b) ZI
A: Alkene converts to epoxide in presence of mcpba. Epoxide can be transformed into the target material…
Q: 3. If the compound shown is subjected to reaction conditions that will hydrolyze amides one of two…
A: This question is related to the stability of products. More stable products will form Faster. Since…
Q: a. What is the amine and coupling components of this azodye? H,CO- -N=N-
A: By seeing the structural and substitution pattern in the given azodye molecules we can decide the…
Q: Which amines cannot be prepared by the Gabriel synthesis? Explain your choices
A: Gabriel synthesis: Gabriel synthesis is a chemical reaction that transforms an alkyl halide into a…
Draw the major product formed from Hofmann elimination of the following
![[1] CH,I (excess)
NH2
[2] Ag,0
[3] A](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fba19331b-d8f8-4777-bdf3-6588e6ba0e8e%2Fc9eb3d77-153c-464c-9f22-62ae19eed537%2Fbwdfxtc.png&w=3840&q=75)
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- So for part a) I found that k=1.60, but im stuck on part b). For part b) I calculated the concentrations for both H2 and CO2, which gave me 0.025mol/L, after that I dont know what to do. Thank you.1,5419 g of magnetite (Fe3O4) ore; Fe+2 and Fe + 3 in concentrated HCL to form a mixtureit's unraveling. Adding HNO3 to all Fe +2s Fe +3 e and Fe+3 s NH, addingwith Fe(OH)3, precipitating into. Sediment in the form of Fe3O4 after necessary operationsand 0.8525 g. Calculate the percentage of Fe3O4 in the sample.Sagrm
- Toxic Cr(VI) can be precipitated from an aqueous solution by bubbling SO2 through the solution. How much SO2 is required to treat 3.00x10^8L of 4.00x10^-2 mM Cr(VI)? 2CrO4^-2 + 3SO2 + 4H^+ —> Cr2(SO4)3 + 2H2O ___kgWhat is the balanced equation for the combustion of C8H7NO2SBrCl in aC,H,N,S elemental analyzer?0.1724g of a mineral containing MnO₂ was dissolved and then treated with excess iodide according to the following unbalanced reaction: MnO2(s) + H+ → Mn²+ + I2 + H₂O The I₂ released was titrated with a solution of Na₂S2O3 0.07320 mol/L, requiring 14.65 mL to reach the point end of degree a) Determine the percentage of MnO₂ in the ore. b) When iodine solutions are used as titrants these are prepared by dissolving 1₂ in concentrated KI. Explain the reason for the need for KI in the preparation of these solutions?
- Kp of this quation 2A+3B=4C+5D2. An analysis for borohydride ion is based on its reaction with Ag+: BH4 - + 8Ag+ + 8OH- -> H2BO3 - + 8Ag(s) + 5H2O The purity of a quantity of KBH4 to be used was established by diluting 3.213 g of the material to exactly 500.0 mL, treating a 100.0-mL aliquot with 50.00 mL of 0.2221 M AgNO3, and titrating the excess silver ion with 3.36 mL of 0.0397 M KSCN. Calculate the percent purity of the KBH4 (53.941 g/mol).1. A newly discovered iron ore was weighted (5.408 g) and worked up to produced 0.3785 g of ignited Fe2O3 precipitate. What is the percent purity of the iron in the sample? 2. Distinguish between equivalence point and end point.