Q: All primary amines can be utilized to initiate a diazotization process. True or False
A: In diazotization reaction, the nitrous acid reacts with aromatic amines to yield the diazonium salt.
Q: (1) Which is the most basic amine and which is a secondary amine? (2) Which can undergo hydrolysis?…
A: Given (1) Which is the most basic amine and which is a secondary amine? (2) Which can undergo…
Q: Write the mechanism for the following reactions:1. the acid-catalyzed hydrolysis of an imine to a…
A: Introduction: An imine is a functional group having carbon-nitrogen double bond and enamine is a…
Q: a) Show the mechanism of synthesis of an amide from an ester and a primary amine: b) The ester…
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Q: Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSE…
A: Statement 1: Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination…
Q: Esters have two unique sides. When looking at an nmr spectrum the hydrogens alpha to the carbonyl…
A: Esters have two NMR active Hydrogens 1) Alpha to Carbonyl Carbon 2) Alpha to Oxygen atom of Ester…
Q: Give the products expected when the following tertiary amines are treated with a peroxyacid and…
A: The structure of N,N-diethylhexan-2-amine is,
Q: Which amines cannot be prepared by a Gabriel synthesis? Explain your choices. NH2 NH2 NH2 а. b. C.…
A: Gabriel's phthalimide synthesis is used for the conversion of primary alkyl halide into primary…
Q: Which of the following is FALSE about the reaction below? +0₂N NH₂ Select one: Oa. It is initiated…
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Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium salt when it reacts with…
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Q: Which sequence of reactions will convert benzene to 3-chloroaniline in a reasonable yield? (Hint: a…
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Q: Maleic Acid + Bromine à racemic-2,3-Dibromosuccinic Acid Explain the mechanism and reaction
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Q: Show how Gabriel syntheses are used to prepare the following amines.(a) benzylamine
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Q: ELOČOET H2N EtO 'N. H + ELOH Reactions of a primary or secondary amine with diethyl carbonate under…
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Q: The reaction of an ester with an amine is not as slow as the reaction of an ester with water or an…
A: Since you have posted a multiple question, we will solve first one for you. To get remaining…
Q: What is the problem with running the following reaction? NH2 HNO3 H2SO4 It will result in multiple…
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Q: Which of the following functional groups will react faster and at lower conditions to a nucleophilic…
A: Given Choices a. Carboxylic acid b. Nitrile c. Acyl Halide d Ester Functional Group will react…
Q: Which acid anhydride will produce these two products after hydrolysis? OH + OH de ole Compound 1…
A: We have to predict the acetic anhydride
Q: Reaction Scheme (starting materials, reagents, product; this is NOT a curved arrow MECHANISM) ->…
A: The final structure of the prepared direct and disperse azo dye has to be given. Given detail…
Q: Rank the following compounds in order of increasing basicity: L p-nitroaniline H.…
A: Basicity of a molecule is the tendency to donate the lone pair of electrons. Electron withdrawing…
Q: Explain the mechanism for the acid catalyzed hydrolysis of an amide?
A: Amides are the chemical compounds that are obtained by the condensation reactions of carboxylic and…
Q: What carbonyl and nitrogen compounds are needed to make attached compound by reductive amination?…
A: Reductive amination is the synthesis of amines from aldehydes and ketones. For the given compound…
Q: Which acid anhydride will produce these two products after hydrolysis? ОН +
A: Given:
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: Draw the product of attached reductive amination reaction.
A: The product of the above reductive amination reaction is drawn below,
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: Which of the following statements is correct? An aldehyde can react with a secondary amine through a…
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Q: DIN a secondary amine gives a diazonium salt upon reaction with HNO₂, HCI at 0°C can undergo…
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Q: Excess ammonia must be used when a primary amine is synthesized by reductive amination. What product…
A: Synthesis of primary amine by reductive elimination takes place as follows:
Q: Show how to synthesize the following amines from the indicated starting materials byreductive…
A: To synthesize N-Cyclohexylaniline from cyclohexanone The primary amine can be synthesized from the…
Q: Reduction of aromatic nitro-compounds using Sn and HCl gives :Select one a. aromatic secondary…
A: Given, Reduction of aromatic nitro compounds using Sn and HCl gives = ? Sn/HCl - is a reducing agent…
Q: Match each item to a choice: Choices: alkene Reductive amination Curtius rearrangement Hoffman…
A: Match the following of amine reactions
Q: Show how to synthesize the following amines from the indicated starting materials.(a)…
A: Amines are the compounds that have NH2 group present in it. The lone pair of nitrogen can be donated…
Q: Show how to synthesize the following amines from the indicated starting materials byreductive…
A: Amines are the organic molecule contains one or more nitrogen atom. Reductive amination is the…
Q: Show how to synthesize the following amines from the indicated starting materials byreductive…
A: Concept introduction: The reaction of a primary amine with either aldehydes or ketones in the…
Q: Please complete the following synthesis. via reductive amination; provide two methods. each method…
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Q: What alkyl bromide would you use in a Gabriel synthesis to prepare each of the following amines? a.…
A: a.
Q: Show how you can synthesize the following tertiary amine three different ways, each using a…
A: SOLUTION: Step 1: The different methods in which a tertiary amine can be synthesized using a…
Q: Give the products expected when the following tertiary amines are treated with a peroxyacid and…
A: The formation of expected products, when tertiary amines are reacted with a peroxy acid and heated…
Q: What carbonyl and nitrogen compounds are needed to make attached compound by reductive amination?…
A: Reductive amination is the conversion of carbonyl compound into amine in the presence of reducing…
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: the scheme shown consists of key steps in the acidic hydrolysis of an amide. Complete the mechanism…
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Q: Answer both parts plz. Part a) Draw arrow pushing mechanism. Part b) Compare the reactivity of…
A: a) The arrow pushing mechanism for the given reaction is shown below,
Q: Show how to synthesize the following amines from the indicated starting materials byreductive…
A: It is organic chemical reactions shown below
Q: a. Write the mechanism for the following reactions:1. the acid-catalyzed hydrolysis of an imine to a…
A: To find: the acid-catalyzed hydrolysis of an imine to a carbonyl compound and a primary amine 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…
Q: Imine hydrolysis is rapid under strongly acidic conditions (H2O,1 equivalent HCI), but imine…
A: Ans
What is the main reaction mechanism for this reductive
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- Please explain why this reaction will NOT WORK. NO2 1. HNO3, H2SO4, 2. EtCI, AICI3Select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed. 'H Š H O H₂O OH @ 1. NaOH, heat 2. Neutralizing work-up 1 H3O+ O TSOH, H₂O O H a A B C D E HOCH2CH2CH₂OH NaOH HOCH2CH2CH₂OH TSOH HOCH2CH2CH₂OH H₂O TSOH, H₂O CH₂OH(2 eq) TSOHWhat results from the reaction shown? ОН H H CH;OH но- но. OH cat. HC1 OH OH H OCH; H |-0 H H А) НО но. B) H;CO OCH3 H OH H;CO. он HH;COH OCH; OCH; H H H С) Но- но. D) H;CO H;CO. OCH HHH;COH
- The product (s) of the following solvolysis reaction is H. H- H. H. H. HO. H2O/HEAT H. Br Он но H. H. OH II III O II 50% I & 50% ||1) NABH, 2) H3O* O no reaction OH HO TH. HOThe reactants and products for a chemical reaction are shown below. Which arrow pushing mechanism (A-E) would lead to the product that is shown? OE C OD B OA HO A. B. C. D. E. H-O: H-O: H- -H® H-O: 0 H-O: IOH OH + HO
- + F₂ catalyst The above reactants would undergo a catalyst .ل= + H H The above reaction would be an example of HHHH |||| H-C=C-C-C-C-C-H+2H-H | | | | HHHH The above reactants would undergo a(n) catalyst reaction ◆ reaction Isopropyl alcohol (propan-2-ol) is used as a solvent for industrial processes, a disinfectant solution, and a de-icer solution for vehicles. One method of producing isopropyl alcohol is to react propene with water in the presence of an acid catalyst. This reaction is classified as a(n) ◆ reaction.R Br HBr R ? Hint HBr, H₂O₂ R Br OHwhich is the correct reaction?
- The reaction below is a reaction. HBr + KOH H2O + KBr -->? Predict a reactant: ? H₂O™ H₂O™ x=00Question 4 of 4 > O Macmillan Learning Select the best conditions for the reactions. A. H3C CH3 Br Identify the best conditions for Reaction A. NaOCH3, DMSO H+, NaOCH₁, CH₂OH H+, NaOCH₂, DMSO O CH₂OH, heat O NaOCH3, CH, OH H3C CH3 CH3