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For the following questions use these compounds as your choices Cl...
Draw the organic products of the following below reactions Please answer the following questions - 11...
Draw the organic products of the following below
reactions
Please answer the following questions - 11 &12
Slide 10
14. Draw the organic product of the following reactions. NaOH OH SOCl2 OH 800°C OH 11. Why do aldehydes and ketones undergo nucleophilic addition undergo nucleophilic substitution? and carboxylic acid derivatives lain the reactivity trend shown in Slide 10 (acid chlorides>anhydridessestersoamides). Relative Reactivity of Carboxylic Acid Derivatives Substitution in Synthesis Nucleophiles react more readily with unhindered carbonyl groups More electrophilic carbonyl...
please give correct answers to these 5 questions with explanations, thankyou Which solvent(s) is required for...
please give correct answers to these 5 questions with
explanations, thankyou
Which solvent(s) is required for a nucleophilic addition reaction involving a Grignard reagent and a carbonyl compound? What is the primary organic product of the following reaction? н* Select one: +H2N. All reactions must be carried out in water All reactions must be carried out in dry solvents (free of water, for example diethyl ether). Select one There will be no reaction An initial reaction must be carried in...
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2...
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2 elimination d SN2 Nucleophilic substitution e-Electrophilic aromatic substitution f Carbonyl nucleophilic addn g Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. 1.8% Hyc's、CH, + H CH3 2. N(CHs CI a Proton transfer b-Lewis acid/base E2...
Can you check my answers please? To answer the questions below use the following information: Cyanohydrins...
Can
you check my answers please?
To answer the questions below use the following information: Cyanohydrins are important intermediates in the synthesis of c-hydroxycarboxylic acids from ketones and aldehydes. The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid. Nitriles can also be hydrolyzed to carboxylic acids using aqueous base. Unfortunately, when a cyanohydrin is treated with aqueous base the original carbonyl compound is isolated OH CHCOOH HO CN OBU H HCEN H NAOH H20...
PLEASE ANSWER ALL PARTS Part B Which of the following reactions would benefit the most from...
PLEASE ANSWER ALL PARTS
Part B Which of the following reactions would benefit the most from general-acid catalysis? View Available Hint(s) O the reaction of an acyl chloride with water O nucleophilic substitution of an alkyl halide by an amine O nucleophilic addition of water to an ester O nucleophilic substitution of an alkyl chloride by iodide O nucleophilic substitution of an alkyl chloride by water Submit Part E Which of the following is not a true statement? O A...
please help in all sections asap!! In a Clemmensen reduction, an aryl ketone is reduced to...
please help in all sections asap!!
In a Clemmensen reduction, an aryl ketone is reduced to an Oaryl aldehyde Caryl alkane aryl carboxylic acid aryl ester aryi anhydride Identify the electrophile for the Friedel-Crafts acylation of benzene. O aluminum tetrachloride anion aluminum chloride acylium ion carbocation carbanion Which of the following criteria is necessary for a nucleophilic aromatic substitution reaction? © A. The ring must contain a very strong electron withdrawing group. B. The ring must contain a leaving group....
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1...
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1 2 a Enter the number of the compound that could undergo Nucleophilic Aromatic Substitution here b Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here c Explain why it will not undergo this reaction in the space below d Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here e Explain...
Please answer all questions 6) Identify the correct IUPAC systematic name for the structure below. who...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
please only box one answer for each of these questions. HOH • SOCI + SO, HC...
please only box one answer for each of these questions.
HOH • SOCI + SO, HC a = Proton transfer b = Lewis acid base c = Radical chain substitution d = Radical chain addition e = Electrophilic addition f= E1 Elimination g = E2 Elimination h = Syl Nucleophilic substitution = Sy2 Nucleophilic substitution = Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters - for...
please give correct answer to these 5 questions with explanations if possible, thankyou During a nucleophilic...
please give correct answer to these 5 questions with
explanations if possible, thankyou
During a nucleophilic addition reaction between LiAlHe and a carbonyl compound, what atom is the nucleophile? Select one The proton (H) atom The hydrogen atom of the lithium aluminium hydride. The aluminium atom. The carbon atom of the carbonyl group. The oxygen atom of the carbonyl group Why do carbonyl compounds undergo nucleophilic addition reactions ? Select one: The compound the carbonyl group is reacting with is...
Draw the organic products of the following below
reactions
Please answer the following questions - 11 &12
Slide 10
14. Draw the organic product of the following reactions. NaOH OH SOCl2 OH 800°C OH 11. Why do aldehydes and ketones undergo nucleophilic addition undergo nucleophilic substitution? and carboxylic acid derivatives lain the reactivity trend shown in Slide 10 (acid chlorides>anhydridessestersoamides). Relative Reactivity of Carboxylic Acid Derivatives Substitution in Synthesis Nucleophiles react more readily with unhindered carbonyl groups More electrophilic carbonyl...
please give correct answers to these 5 questions with
explanations, thankyou
Which solvent(s) is required for a nucleophilic addition reaction involving a Grignard reagent and a carbonyl compound? What is the primary organic product of the following reaction? н* Select one: +H2N. All reactions must be carried out in water All reactions must be carried out in dry solvents (free of water, for example diethyl ether). Select one There will be no reaction An initial reaction must be carried in...
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2 elimination d SN2 Nucleophilic substitution e-Electrophilic aromatic substitution f Carbonyl nucleophilic addn g Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. 1.8% Hyc's、CH, + H CH3 2. N(CHs CI a Proton transfer b-Lewis acid/base E2...
Can
you check my answers please?
To answer the questions below use the following information: Cyanohydrins are important intermediates in the synthesis of c-hydroxycarboxylic acids from ketones and aldehydes. The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid. Nitriles can also be hydrolyzed to carboxylic acids using aqueous base. Unfortunately, when a cyanohydrin is treated with aqueous base the original carbonyl compound is isolated OH CHCOOH HO CN OBU H HCEN H NAOH H20...
PLEASE ANSWER ALL PARTS
Part B Which of the following reactions would benefit the most from general-acid catalysis? View Available Hint(s) O the reaction of an acyl chloride with water O nucleophilic substitution of an alkyl halide by an amine O nucleophilic addition of water to an ester O nucleophilic substitution of an alkyl chloride by iodide O nucleophilic substitution of an alkyl chloride by water Submit Part E Which of the following is not a true statement? O A...
please help in all sections asap!!
In a Clemmensen reduction, an aryl ketone is reduced to an Oaryl aldehyde Caryl alkane aryl carboxylic acid aryl ester aryi anhydride Identify the electrophile for the Friedel-Crafts acylation of benzene. O aluminum tetrachloride anion aluminum chloride acylium ion carbocation carbanion Which of the following criteria is necessary for a nucleophilic aromatic substitution reaction? © A. The ring must contain a very strong electron withdrawing group. B. The ring must contain a leaving group....
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1 2 a Enter the number of the compound that could undergo Nucleophilic Aromatic Substitution here b Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here c Explain why it will not undergo this reaction in the space below d Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here e Explain...
Please answer all questions
6) Identify the correct IUPAC systematic name for the structure below. who -CH H A) N-methyl-2-ethyl-5-methyloctanamide B) 6,N-dimethylnonane-3-carboxamide C) 5,N-dimethyl-2-ethyloctanamide D) 2-ethyl-5,N-dimethyloctanamide 7) Which of the following is the most reactive carboxylic acid derivative? A) ester B) anhydride C) nitrile D) acid chloride E) amide 8) Identify the carboxylic acid derivative/s in the structure of Lactimidomycin. HN OH O A) Ester B) Anhydride C) Nitrile D) Imine 9) Arrange the carboxylic acid derivatives below in order...
please only box one answer for each of these questions.
HOH • SOCI + SO, HC a = Proton transfer b = Lewis acid base c = Radical chain substitution d = Radical chain addition e = Electrophilic addition f= E1 Elimination g = E2 Elimination h = Syl Nucleophilic substitution = Sy2 Nucleophilic substitution = Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters - for...
please give correct answer to these 5 questions with
explanations if possible, thankyou
During a nucleophilic addition reaction between LiAlHe and a carbonyl compound, what atom is the nucleophile? Select one The proton (H) atom The hydrogen atom of the lithium aluminium hydride. The aluminium atom. The carbon atom of the carbonyl group. The oxygen atom of the carbonyl group Why do carbonyl compounds undergo nucleophilic addition reactions ? Select one: The compound the carbonyl group is reacting with is...
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