solve the reaction and show mechanism
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solve the reaction and show mechanism
60. Arrange these compounds in order of reactivity for a...
H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the...
H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least reactive compound as compound 5. (5 points) NO2 pada CH SO3H OH 5
Arrange the following compounds in order of DECREASING reactivity with Hoffor HORATE 51 is the MOST...
Arrange the following compounds in order of DECREASING reactivity with Hoffor HORATE 51 is the MOST REACTIVE and 4 is the LEAST REACTIVE) CH,CH, CCH (CH), CHOCH Tonyo, onde on, ouder, CH, CH bor
Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reactions (most...
Rank the following compounds in order of decreasing reactivity
in a nucleophilic acyl substitution reactions (most to least
reactive from left to right in the answer)
yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. Rank the following...
Rank the following carbonyl-containing
compounds in order of reactivity towards nucleophilic acyl
substitution.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive Least reactive butyl acetate benzoic anhydride 3-methylpentanoyl chloride propionamide
III. Correctly arrange the compounds in each set in order of decreasing reactivity toward the indicated...
III. Correctly arrange the compounds in each set in order of decreasing reactivity toward the indicated reaction (most reactive compound first). 1.Alkyl iodide formation with HI: A. 1-hexanol B. tert-butanol C. 2-pentanol D. isopentane Answer: __________ > __________ > __________ > _________. 2. Dehydrationwith catalyticH2SO4: A. cyclopentanol B. 2-methyl-2-hexanol C. methanol D. 1-octanol Answer: __________ > __________ > __________ > _________.
organic chemistry 353 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution...
organic chemistry 353
2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
1. Which of the compounds listed below would you expect to have the highest boiling point? They all have approximately the same molecular weight.) a. CH CH CH CH CH b. CH3CH CH C2OH d. Cl,CH:CH,CI...
1. Which of the compounds listed below would you expect to have the highest boiling point? They all have approximately the same molecular weight.) a. CH CH CH CH CH b. CH3CH CH C2OH d. Cl,CH:CH,CI 2. How many 'H NMR signals would you expect from this compound? d.4 3. Arrange these compounds in order of reactivity for a nucleophilic substitution reaction using CH3O in CH:OH. List the most reactive compound first. a. 3 2> 1 d. 21 3 b....
6. Circle the aromatic compounds from the list below. (5 points) 7. Rank the compounds below...
6. Circle the aromatic compounds from the list below. (5
points)
7. Rank the compounds below in order of reactivity to
Electrophilic Aromatic Substitution. Rank the most reactive
compound as compound 1 and the least reactive compound as compound
5. (5 points)
6. Circle the aromatic compounds from the list below. (5 points) OH :O: H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least...
I need help with to solve this! 1. List the following carbonyl compounds in order of...
I need help with to solve this!
1. List the following carbonyl compounds in order of decreasing reactivity toward nucleophilic attack. CH CH3CH2CHCCCH2CH3 CH3CH2 CHCCH2CH3 CH3CH 2CH CH, CH CH CH3CH2CCH2CH3 CH3CH2CHCCHCH2CH3 CH CHCH CCH CH CH3 CH CH3 2. Each of the 30 alcohols below can be synthesized three different ways starting with a carbonyl compound and a Grignard reagent. Provide those syntheses for each alcohol shown. OH OH CH.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl...
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl chloride hexyl propanoate Least reactive acetic anhydride propionamide
H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least reactive compound as compound 5. (5 points) NO2 pada CH SO3H OH 5
Arrange the following compounds in order of DECREASING reactivity with Hoffor HORATE 51 is the MOST REACTIVE and 4 is the LEAST REACTIVE) CH,CH, CCH (CH), CHOCH Tonyo, onde on, ouder, CH, CH bor
Rank the following compounds in order of decreasing reactivity
in a nucleophilic acyl substitution reactions (most to least
reactive from left to right in the answer)
yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
Rank the following carbonyl-containing
compounds in order of reactivity towards nucleophilic acyl
substitution.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive Least reactive butyl acetate benzoic anhydride 3-methylpentanoyl chloride propionamide
organic chemistry 353
2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
1. Which of the compounds listed below would you expect to have the highest boiling point? They all have approximately the same molecular weight.) a. CH CH CH CH CH b. CH3CH CH C2OH d. Cl,CH:CH,CI 2. How many 'H NMR signals would you expect from this compound? d.4 3. Arrange these compounds in order of reactivity for a nucleophilic substitution reaction using CH3O in CH:OH. List the most reactive compound first. a. 3 2> 1 d. 21 3 b....
6. Circle the aromatic compounds from the list below. (5
points)
7. Rank the compounds below in order of reactivity to
Electrophilic Aromatic Substitution. Rank the most reactive
compound as compound 1 and the least reactive compound as compound
5. (5 points)
6. Circle the aromatic compounds from the list below. (5 points) OH :O: H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least...
I need help with to solve this!
1. List the following carbonyl compounds in order of decreasing reactivity toward nucleophilic attack. CH CH3CH2CHCCCH2CH3 CH3CH2 CHCCH2CH3 CH3CH 2CH CH, CH CH CH3CH2CCH2CH3 CH3CH2CHCCHCH2CH3 CH CHCH CCH CH CH3 CH CH3 2. Each of the 30 alcohols below can be synthesized three different ways starting with a carbonyl compound and a Grignard reagent. Provide those syntheses for each alcohol shown. OH OH CH.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl chloride hexyl propanoate Least reactive acetic anhydride propionamide
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Amplitude=3;
fs=8000;
n=0:399;
t=0:1/fs: n*1/fs-1/fs;
signal=3+3*cos(2*pi*1100*t)+3*cos(2*pi*2200*t)+3*cos(2*pi*3300*t);
fftSignal= fft(signal);
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xlabel('Frequency(Hz)’)
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