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PLEASE ANSWER !! please answer 1,2,and 3. i will give a thumbs up
1.) WHICH OF...
Give Simple, correct answer will give thumbs and good rating Part A aniline Drag the appropriate...
Give Simple, correct answer
will give thumbs and good rating
Part A aniline Drag the appropriate labels to their respective targets. Rese HCI KON Hy0 NO2 NH2 Sn HN03 H2SO4 NaN Bra Part B p-bromoaniline Drag the appropriate labels to their respective targets. Reset C FeBrs H,SO Br HIO Br2 HNO3 Brs NO2 + ortho Fe NH, Submit Request Answer Part C m-bromoaniline Drag the appropriate labels to their respective targets. Reset H2O HCI H,SO NO2 NO2 ةة Sn NO,...
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....
use the notes provided to help answer the question above. will rate well The second step...
use the notes provided to help answer the question
above. will rate well
The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....
please answer every part of question 6!! and i will make sure to thumbs up the answer! 6) a) How many aromatic 'H NM...
please answer every part of question 6!! and i will make sure
to thumbs up the answer!
6) a) How many aromatic 'H NMR signals would be expected for 4-bromo-3-methylanisole? (0.5 pts.) b) What would the expected 'H NMR chemical shift be for the protons of the OCH; group?_ _(0.5 pts.) c) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H. through H., if needed. If the hydrogens are chemically shift...
please answer ALL. will give a thumbs up rating. thank you! Predict the product of the...
please answer ALL. will give a thumbs up rating. thank
you!
Predict the product of the following reaction. OsO4, (CH3)2COOH (CH3)3COH, NaOH С" ОН + enantiomer ОН ОН ОН + enantiomer ОН ОН + enantiomer Predict the product of the following reaction. Ph3P Y о OH OH Predict the product of the following reaction. O 1. MgBr 2. Hz0+ OH + enantiomer о OH + enantiomer OH + enantiomer OH + enantiomer
please answer ALL. will give a thumbs up. thank you! Predict the product of the following...
please answer ALL. will give a thumbs up. thank you!
Predict the product of the following reaction. (CH3)2NH NaBH CN HO NH OH Determine the product of the following reaction. НСІ о ? ОН СІ ОН -ОН CI None of these products will be formed. СІ ОН Predict the product of the following intramolecular Aldol reaction. NaOH, HAO A i H o مل os
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
please answer every part of number 8, i will thumbs up answer! 8) a) How many aromatic 'H NMR signals would be expec...
please answer every part of number 8, i will thumbs up
answer!
8) a) How many aromatic 'H NMR signals would be expected for 2-bromo-5-methylanisole? (0.5 pts.) b) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H, through H , if needed. If the hydrogens are chemically shift equivalent, use the same label for each member of the set of equivalent hydrogens. ΥΗ c) Calculate the chemical shifts for the aromatic...
PLEASE ANSWER ALL. I will give thumbs up and leave a good comment if answers are...
PLEASE ANSWER ALL. I will give thumbs up and leave a good comment
if answers are accurate. NOTE: Please explain clearly in words.
Please be detailed.
The combination of these two carbonyl systems can give an aldol product. Part 1. Will more than one enolate form? Part 2. What kind of base would you use? (NaOH or LDA) Why? Part 3. If you were in the lab running this experiment, which reagent (2,2-dimethylpropanal or phenylacetaldehyde) should you add slowly to...
please answer every part of question 7! I will make sure to thumbs up answer! 7) a) How many aromatic 'H NMR signals...
please answer every part of question 7! I will make sure to
thumbs up answer!
7) a) How many aromatic 'H NMR signals would be expected for 3-bromo-5-methylanisole? (0.5 pts.) b) What the expected integration values be for the two methyl groups for 4-bromo-3-methylanisole? (0.5 pts.) c) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H, through H, if needed. If the hydrogens are chemically shift equivalent, use the same label...
Give Simple, correct answer
will give thumbs and good rating
Part A aniline Drag the appropriate labels to their respective targets. Rese HCI KON Hy0 NO2 NH2 Sn HN03 H2SO4 NaN Bra Part B p-bromoaniline Drag the appropriate labels to their respective targets. Reset C FeBrs H,SO Br HIO Br2 HNO3 Brs NO2 + ortho Fe NH, Submit Request Answer Part C m-bromoaniline Drag the appropriate labels to their respective targets. Reset H2O HCI H,SO NO2 NO2 ةة Sn NO,...
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....
use the notes provided to help answer the question
above. will rate well
The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....
please answer every part of question 6!! and i will make sure
to thumbs up the answer!
6) a) How many aromatic 'H NMR signals would be expected for 4-bromo-3-methylanisole? (0.5 pts.) b) What would the expected 'H NMR chemical shift be for the protons of the OCH; group?_ _(0.5 pts.) c) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H. through H., if needed. If the hydrogens are chemically shift...
please answer ALL. will give a thumbs up rating. thank
you!
Predict the product of the following reaction. OsO4, (CH3)2COOH (CH3)3COH, NaOH С" ОН + enantiomer ОН ОН ОН + enantiomer ОН ОН + enantiomer Predict the product of the following reaction. Ph3P Y о OH OH Predict the product of the following reaction. O 1. MgBr 2. Hz0+ OH + enantiomer о OH + enantiomer OH + enantiomer OH + enantiomer
please answer ALL. will give a thumbs up. thank you!
Predict the product of the following reaction. (CH3)2NH NaBH CN HO NH OH Determine the product of the following reaction. НСІ о ? ОН СІ ОН -ОН CI None of these products will be formed. СІ ОН Predict the product of the following intramolecular Aldol reaction. NaOH, HAO A i H o مل os
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
please answer every part of number 8, i will thumbs up
answer!
8) a) How many aromatic 'H NMR signals would be expected for 2-bromo-5-methylanisole? (0.5 pts.) b) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H, through H , if needed. If the hydrogens are chemically shift equivalent, use the same label for each member of the set of equivalent hydrogens. ΥΗ c) Calculate the chemical shifts for the aromatic...
PLEASE ANSWER ALL. I will give thumbs up and leave a good comment
if answers are accurate. NOTE: Please explain clearly in words.
Please be detailed.
The combination of these two carbonyl systems can give an aldol product. Part 1. Will more than one enolate form? Part 2. What kind of base would you use? (NaOH or LDA) Why? Part 3. If you were in the lab running this experiment, which reagent (2,2-dimethylpropanal or phenylacetaldehyde) should you add slowly to...
please answer every part of question 7! I will make sure to
thumbs up answer!
7) a) How many aromatic 'H NMR signals would be expected for 3-bromo-5-methylanisole? (0.5 pts.) b) What the expected integration values be for the two methyl groups for 4-bromo-3-methylanisole? (0.5 pts.) c) Proceeding in a clockwise direction, label each unique hydrogen atom on the aromatic ring using the labels H, through H, if needed. If the hydrogens are chemically shift equivalent, use the same label...
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