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LIST IN ORDER OF REACTIVITY TOWARD NUCLEOPH) LC ATTACK Нs cs ? с. CH3 CH2 CHS...
The following phosgene substitutes are shown in order of decreasing reactivity toward nucleophilic attack. Explain this order...
The following phosgene substitutes are shown in order of decreasing reactivity toward nucleophilic attack. Explain this order of reactivity.
1) Name the following compounds, according to IUPAC rules: (20 pts.) a) b) CH3-CH2 CEC-CH-CH2-CH-CHs d)...
1) Name the following compounds, according to IUPAC rules: (20 pts.) a) b) CH3-CH2 CEC-CH-CH2-CH-CHs d) CH3 CH-CH-CH2-CH2-CH сH, CH3 e) CH3 CH3-C C-CH2-CH-CH2- CH3 f) CH3 -CH2-CH2-CH3 CH3-CH CH-CH-CH2 g) CH3 н - c-c CH-CH2-CH2 CH3 CH3 н i) -CHз CI Hас CH3-C CH2-CH3 CI j) CH2-CH3 "CH,—сн, CH2 CH3
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack,...
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack, by inputing a ranking number (1-4) in the box next to each structure (most reactive-1).
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.
Consider the following molecules: b. а. CHS CH3 O NH— CH—CH2—ОН NH2-CH-C-OH CHз d. C. CHз...
Consider the following molecules: b. а. CHS CH3 O NH— CH—CH2—ОН NH2-CH-C-OH CHз d. C. CHз о Но-СН—С—ОН НО—С—С—С—ОН CH3 [Select ] i. Which of the molecules above is a secondary amine? ii. Which of the molecules above will be a zwitterion under physiological conditions (pH 7)? (Select) [Select ] ii. Which of the molecules above has two acidic protons?
Based on their composition and structure, list CH COCHs, CH3 CH2 CH3, and CH3 COOH in...
Based on their composition and structure, list CH COCHs, CH3 CH2 CH3, and CH3 COOH in order of decreasing intermolecular forces. Rank the compounds from strongest to weakest intermolecular forces. To rank items as equivalent, overlap them. Reset Help CH3COCH3 CH3 CH2CH3 CH3 COOH Strongest Weakest The correct ranking cannot be determined
List the following compounds in order of increasing reactivity in an E1 elimination. CH3CH2CHBrCH3, CH3CH2CH2CH2Br, (CH3)3CBr
List the following compounds in order of increasing reactivity in an E1 elimination. CH3CH2CHBrCH3, CH3CH2CH2CH2Br, (CH3)3CBr
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе mos...
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
29/ The main product of CH3(CH2),COOH 1) LiAlH, 2) H30* А CH3CH2CH2CH2CH; B CH(CH, CHẠCHO С....
29/ The main product of CH3(CH2),COOH 1) LiAlH, 2) H30* А CH3CH2CH2CH2CH; B CH(CH, CHẠCHO С. CH3(CH),CHOH D OH CH,CH,CHCH.CH
At 500 ∘C, cyclopropane (C3H6) rearranges to propene (CH3−CH=CH2). The reaction is first order, and the...
At 500 ∘C, cyclopropane (C3H6) rearranges to propene (CH3−CH=CH2). The reaction is first order, and the rate constant is 6.7×10−4s−1. If the initial concentration of C3H6 is 5.50×10−2 M . What is the molarity of C3H6 after 30 min ? How many minutes does it take for the C3H6 concentration to drop to 1.00×10−2 M ? How many minutes does it take for 25% of the C3H6 to react? Express all the answers in two significant figures.
1) Name the following compounds, according to IUPAC rules: (20 pts.) a) b) CH3-CH2 CEC-CH-CH2-CH-CHs d) CH3 CH-CH-CH2-CH2-CH сH, CH3 e) CH3 CH3-C C-CH2-CH-CH2- CH3 f) CH3 -CH2-CH2-CH3 CH3-CH CH-CH-CH2 g) CH3 н - c-c CH-CH2-CH2 CH3 CH3 н i) -CHз CI Hас CH3-C CH2-CH3 CI j) CH2-CH3 "CH,—сн, CH2 CH3
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack, by inputing a ranking number (1-4) in the box next to each structure (most reactive-1).
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.
Consider the following molecules: b. а. CHS CH3 O NH— CH—CH2—ОН NH2-CH-C-OH CHз d. C. CHз о Но-СН—С—ОН НО—С—С—С—ОН CH3 [Select ] i. Which of the molecules above is a secondary amine? ii. Which of the molecules above will be a zwitterion under physiological conditions (pH 7)? (Select) [Select ] ii. Which of the molecules above has two acidic protons?
Based on their composition and structure, list CH COCHs, CH3 CH2 CH3, and CH3 COOH in order of decreasing intermolecular forces. Rank the compounds from strongest to weakest intermolecular forces. To rank items as equivalent, overlap them. Reset Help CH3COCH3 CH3 CH2CH3 CH3 COOH Strongest Weakest The correct ranking cannot be determined
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
29/ The main product of CH3(CH2),COOH 1) LiAlH, 2) H30* А CH3CH2CH2CH2CH; B CH(CH, CHẠCHO С. CH3(CH),CHOH D OH CH,CH,CHCH.CH
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