Which Allene is the most stable ? How do I go about solving a problem like this ?
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usually , if the no of branches increases on double bond carbon, the stability increases.
so that ,
answer : A
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Which Allene is the most stable ? How do I go about solving a
problem like...
Which Allene is least stable? Which alkene is least stable? A I B) II C) III...
Which Allene is least stable?
Which alkene is least stable? A I B) II C) III D None of these
Draw most stable chair form for the more stable stereoisomer for the molecule. All help is...
Draw most stable chair form for the more stable stereoisomer
for the molecule. All help is appreciated
yclohexane Chair Practice 9. For each of the following do two things: A draw the most stable chair form for the more stable stereoisomer for the molecule B. identify whether the more stable stereoisomer is cis or trans. 7. 1-butyl-2-methylcyclohexane 8. 3-t-butyl-1-methylcyclohexane 9. 1,4-diethylcyclohexane C. For each of the following, do two things: A draw the most stable chair form over groups C...
How do I go about solving this problem in R? # This is a challenge. Essentially,...
How do I go about solving this problem in R?
# This is a challenge. Essentially, you will use loops to calculate the # sum of the sequence: 4/1 - 4/3 + 4/5 - 4/7 + 4/9 - 4/11... # Use a for loop and if statements as needed. Store the sum in the # object 'result'. # Once your code works, increase iterations to 10000+ and see what you get. # Hints: # - use an object called "add"...
According to YOUR EXPERIMENTAL OBSERVATIONS, which isomer of 1, 4-diphenyl-2-butene-1, 4-dione is more stable? Explain how...
According to YOUR EXPERIMENTAL OBSERVATIONS, which isomer of 1, 4-diphenyl-2-butene-1, 4-dione is more stable? Explain how you arrived at your answer. Which of the two definitions of stability in the "Principles" section did you use? Is your answer consistent with the findings of other chemists on the relative stabilities of cis and trans alkene isomers? Give the reference you used to obtain the needed information. What experimental observations DID YOU MAKE which support the theory that there is restricted rotation...
How would I go about solving parts 2,3, and 4 in this problem? How would I...
How would I go about solving parts 2,3, and 4 in this
problem? How would I draw the product?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., SN1, SN2, El, or E4), draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate rxn....
i know that trans is more stable than cis but i really confusion between 2 and...
i know that trans is more stable than cis but i really
confusion between 2 and 4. please give me the answer with clear
explanation and clear writing.
i dont know anything about bulky group
5. Which of the following is the most stable conformation of trans-1-ethyl-3-methylcyclohexane? CH.CH CH2CH3 ÇH CH3 CH3 CH2CHE CH2CHE - C O (A) 1 (B)2 O(C) 3 O (D) 4
I'm a bit unsure on how I would go about solving this. The incline made a...
I'm a bit unsure on how I would go about solving this. The
incline made a 25-degree angle under the thunderstorm area, and the
rest of the measurements can be seen in the image, but I don't
think I collected enough information. Any suggestions on how to
solve a problem like this (even if there isn't an answer available)
would be appreciated. Will rate.
In an amusement park ride, a roller coaster car carries screaming patrons down a steep incline....
How does part b differ from part a and how do I go about solving this?...
How does part b differ from part a and how do I go about
solving this?
Preparing for the lab: Exercise #3 Your TA asks you to make 100 mLof a benzoic acidbenzoate buffer solution of pH 4.40. The Ka of benzoic acid is 6.5 x 10 s. a) Determine the volumes of 0.50 M benzoic acid and 0.50 M sodium benzoate required to make 100.0 mL of a pH 4.40 buffer solution. b) Determine the volumes of0.50 M benzoic...
Why’s is choice IV the most stable in question 4 and for question 5 where do...
Why’s is choice IV the most stable in question 4 and for
question 5 where do I place all components of the conformer
4. Which would be the most stable conformation of trans-1-me ? Why? CH CH3 CH Bu Bu Bu IV H 5. Using the chair conformations drawn below, give the most stable and the least stable conformations of cls- and trans- 1-isobutyl-2-ethylcyclohexane. Show to which side the equilibrium lies and briefly explain why
please help 4. For each pair of structures below circle the most relatively stable one. Show...
please help
4. For each pair of structures below circle the most relatively stable one. Show work by drawing relevant chair structures and/or Newman projections as needed) to clearly illustrate why. It is best practice here that only the most stable conformations for each compound are being compared in each set. For clarity. provide a few words that explain your analysis when comparing the illustrations. (12pts total for this problem) (a) ♡ va ♡ 5. (a) (3pts) Look up trans-decalin...
Which Allene is least stable?
Which alkene is least stable? A I B) II C) III D None of these
Draw most stable chair form for the more stable stereoisomer
for the molecule. All help is appreciated
yclohexane Chair Practice 9. For each of the following do two things: A draw the most stable chair form for the more stable stereoisomer for the molecule B. identify whether the more stable stereoisomer is cis or trans. 7. 1-butyl-2-methylcyclohexane 8. 3-t-butyl-1-methylcyclohexane 9. 1,4-diethylcyclohexane C. For each of the following, do two things: A draw the most stable chair form over groups C...
How do I go about solving this problem in R?
# This is a challenge. Essentially, you will use loops to calculate the # sum of the sequence: 4/1 - 4/3 + 4/5 - 4/7 + 4/9 - 4/11... # Use a for loop and if statements as needed. Store the sum in the # object 'result'. # Once your code works, increase iterations to 10000+ and see what you get. # Hints: # - use an object called "add"...
According to YOUR EXPERIMENTAL OBSERVATIONS, which isomer of 1, 4-diphenyl-2-butene-1, 4-dione is more stable? Explain how you arrived at your answer. Which of the two definitions of stability in the "Principles" section did you use? Is your answer consistent with the findings of other chemists on the relative stabilities of cis and trans alkene isomers? Give the reference you used to obtain the needed information. What experimental observations DID YOU MAKE which support the theory that there is restricted rotation...
How would I go about solving parts 2,3, and 4 in this
problem? How would I draw the product?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., SN1, SN2, El, or E4), draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate rxn....
i know that trans is more stable than cis but i really
confusion between 2 and 4. please give me the answer with clear
explanation and clear writing.
i dont know anything about bulky group
5. Which of the following is the most stable conformation of trans-1-ethyl-3-methylcyclohexane? CH.CH CH2CH3 ÇH CH3 CH3 CH2CHE CH2CHE - C O (A) 1 (B)2 O(C) 3 O (D) 4
I'm a bit unsure on how I would go about solving this. The
incline made a 25-degree angle under the thunderstorm area, and the
rest of the measurements can be seen in the image, but I don't
think I collected enough information. Any suggestions on how to
solve a problem like this (even if there isn't an answer available)
would be appreciated. Will rate.
In an amusement park ride, a roller coaster car carries screaming patrons down a steep incline....
How does part b differ from part a and how do I go about
solving this?
Preparing for the lab: Exercise #3 Your TA asks you to make 100 mLof a benzoic acidbenzoate buffer solution of pH 4.40. The Ka of benzoic acid is 6.5 x 10 s. a) Determine the volumes of 0.50 M benzoic acid and 0.50 M sodium benzoate required to make 100.0 mL of a pH 4.40 buffer solution. b) Determine the volumes of0.50 M benzoic...
Why’s is choice IV the most stable in question 4 and for
question 5 where do I place all components of the conformer
4. Which would be the most stable conformation of trans-1-me ? Why? CH CH3 CH Bu Bu Bu IV H 5. Using the chair conformations drawn below, give the most stable and the least stable conformations of cls- and trans- 1-isobutyl-2-ethylcyclohexane. Show to which side the equilibrium lies and briefly explain why
please help
4. For each pair of structures below circle the most relatively stable one. Show work by drawing relevant chair structures and/or Newman projections as needed) to clearly illustrate why. It is best practice here that only the most stable conformations for each compound are being compared in each set. For clarity. provide a few words that explain your analysis when comparing the illustrations. (12pts total for this problem) (a) ♡ va ♡ 5. (a) (3pts) Look up trans-decalin...
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