Explain whether you would expect 2,5-dichloro-2,5-dimethylhexane to react with 18% sodium iodide in acetone. If a...
Explain whether you would expect 2,5-dichloro-2,5-dimethylhexane to react with 18% sodium iodide in acetone. If a reaction is expected, and draw the product that is likely to be formed in the reaction.
Explain whether you would expect 2,5-dichloro-2,5-dimethylhexane to react with 1% silver nitrate in ethanol. If a reaction is expected, and draw the product that is likely to be formed in the reaction.
Homework Answers
In first case solvent is acetone that is Polar aprotic solvent. so tertiary alkyl halide will undergo SN2 reaction at a very slow rate because Acetone is used for SN2 reaction.
while in case of second we have ethanol that is Polar protic solvent. Polar protic solvent stabilize the tertiary carbon cation formed after Cl- removal. so reaction occurs very fast to form curdy white ppt. Of Agcl.
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Explain whether you would expect 2,5-dichloro-2,5-dimethylhexane
to react with 18% sodium iodide in acetone. If a...
Two unknown compounds were tested in a sodium iodide in acetone test and a silver nitrate...
Two unknown compounds were tested in a sodium iodide in acetone test and a silver nitrate in ethanol test. The observations of these tests are given below. Use structures A-E to the right to answer the following questions. Given these observations, what are the identities of Unknowns 1 and 2? Unknown 1 Unknown 2 Do you except reaction of bromobenzene (B) in the silver nitrate in ethanol test to be fast, slow or nonreactive? Why? Do you except Structure E...
. . . . 2.Write the chemical reaction of the following: Sodium Iodide in acetone with...
. . . . 2.Write the chemical reaction of the following: Sodium Iodide in acetone with 1-Bromobutane Sodium Iodide in acetone with 1- Chlorobutane Sodium Iodide in acetone with 2-Bromobutane Sodium Iodide in acetone with 2-Chlorobutane Sodium Iodide in acetone with 1-Chloro-2-methyl pentane Silver Nitrate in alcohol with 1-Bromobutane Silver Nitrate in alcohol with 1- Chlorobutane Silver Nitrate in alcohol with 2-Bromobutane SIlver Nitrate in alcohol with 2-Chlorobutane Silver Nitrate in alcohol with 1-Chloro-2-methyl pentane . . . . .
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with...
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2 gniqmo silver nitrate in ethanol, conditions. Please explain.gO o vioieV a to 2iivitorsl S Br bas wonnuwoy linsbl oeuloco eh or m poy wol i Br
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2...
In lab you will be performing experiments using Sodium (or Potassium) Iodide in Acetone to determine...
In lab you will be performing experiments using Sodium (or Potassium) Iodide in Acetone to determine reactivity in SN1 reactions and Silver Nitrate in Ethanol to investigate SN2 reactions. How will you know if an alkyl halide is moderately reactive in either test?
indicate which reaction will occur faster. explain your reasoning. reaction of 1 chlorobutane with sodium iodide...
indicate which reaction will occur faster. explain
your reasoning. reaction of 1 chlorobutane with sodium iodide or
sodium p toluenesulfonate in aqueous ethanol.
Indicate which reaction will occur faster. Explain your reasoning. Select the single best answer Reaction of 1-chlorobutane with sodium iodide or sodium p-toluenesulfonate in aqueous ethanol Sodium iodide will react faster because the leaving group encounters less sterle hindrance. Sodium iodide will react faster because the intermediate is more stabilized in the solvent. Sodium p-toluenesulfonate will react...
please help! will rate! white boxes beed to be filled in & Im struggling with questions...
please help! will rate! white boxes beed to be filled in & Im
struggling with questions 1-3 thank you!!
1. Balance the following reaction equation. Note: in Organic Chemistry, a standard balanced reaction equation not only balances all the elements on the left vs. the right, but also shows molecular structures. Formulas such as "C.H.O." are normally not used, because they don't identify a specific isomer. conc. HCI conc. HCI X 2. Complete the following table, using your actual measured...
i need help with balancing the equation in question 1 in the first picture and answering...
i need help with balancing the equation in question 1 in the
first picture and answering number 1 in the second picture please
as soon as possible
1. Balance the following reaction equation. Note: in Organic Chemistry, a standard balanced reaction equation not only balances all the elements on the left vs. the right, but also shows molecular structures. Formulas such as "CHO." are normally not used, because they don't identify a specific isomer. conc. HCI 2. Complete the following...
5- Draw the mechanism of the below reaction when 1. The Nu' is sodium iodide dissolved...
5- Draw the mechanism of the below reaction when 1. The Nu' is sodium iodide dissolved in acetone II. The Nuis sodium iodide dissolved in ethanol What do you do to speed the reaction rate in both reactions? (1.5 points) Nu :
17. Draw the entire mechanism that outlines the reaction of sodium borohydride with acetone. 18. Draw...
17. Draw the entire mechanism that outlines the reaction of sodium borohydride with acetone. 18. Draw the entire mechanism of the acid-catalyzed reaction of ethanol with acetic acid. 19. Draw the entire mechanism of the reaction of methylmagnesium bromide with acetone. 20. SPIDER. Starting with 2-butanol, identify at least 4 reactions that you can think of with this compound (either as the starting material or the product). Then, identify at least 2 reactions for each of the compounds you draw.
Which of the follow would you expect to react fastest with silver nitrate in ethanol? primary alkyl bromide primar...
Which of the follow would you expect to react fastest with silver nitrate in ethanol? primary alkyl bromide primary alkyl chloride secondary alkyl chloride tertiary alkyl bromide
Two unknown compounds were tested in a sodium iodide in acetone test and a silver nitrate in ethanol test. The observations of these tests are given below. Use structures A-E to the right to answer the following questions. Given these observations, what are the identities of Unknowns 1 and 2? Unknown 1 Unknown 2 Do you except reaction of bromobenzene (B) in the silver nitrate in ethanol test to be fast, slow or nonreactive? Why? Do you except Structure E...
. . . . 2.Write the chemical reaction of the following: Sodium Iodide in acetone with 1-Bromobutane Sodium Iodide in acetone with 1- Chlorobutane Sodium Iodide in acetone with 2-Bromobutane Sodium Iodide in acetone with 2-Chlorobutane Sodium Iodide in acetone with 1-Chloro-2-methyl pentane Silver Nitrate in alcohol with 1-Bromobutane Silver Nitrate in alcohol with 1- Chlorobutane Silver Nitrate in alcohol with 2-Bromobutane SIlver Nitrate in alcohol with 2-Chlorobutane Silver Nitrate in alcohol with 1-Chloro-2-methyl pentane . . . . .
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2 gniqmo silver nitrate in ethanol, conditions. Please explain.gO o vioieV a to 2iivitorsl S Br bas wonnuwoy linsbl oeuloco eh or m poy wol i Br
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2...
indicate which reaction will occur faster. explain
your reasoning. reaction of 1 chlorobutane with sodium iodide or
sodium p toluenesulfonate in aqueous ethanol.
Indicate which reaction will occur faster. Explain your reasoning. Select the single best answer Reaction of 1-chlorobutane with sodium iodide or sodium p-toluenesulfonate in aqueous ethanol Sodium iodide will react faster because the leaving group encounters less sterle hindrance. Sodium iodide will react faster because the intermediate is more stabilized in the solvent. Sodium p-toluenesulfonate will react...
please help! will rate! white boxes beed to be filled in & Im
struggling with questions 1-3 thank you!!
1. Balance the following reaction equation. Note: in Organic Chemistry, a standard balanced reaction equation not only balances all the elements on the left vs. the right, but also shows molecular structures. Formulas such as "C.H.O." are normally not used, because they don't identify a specific isomer. conc. HCI conc. HCI X 2. Complete the following table, using your actual measured...
i need help with balancing the equation in question 1 in the
first picture and answering number 1 in the second picture please
as soon as possible
1. Balance the following reaction equation. Note: in Organic Chemistry, a standard balanced reaction equation not only balances all the elements on the left vs. the right, but also shows molecular structures. Formulas such as "CHO." are normally not used, because they don't identify a specific isomer. conc. HCI 2. Complete the following...
5- Draw the mechanism of the below reaction when 1. The Nu' is sodium iodide dissolved in acetone II. The Nuis sodium iodide dissolved in ethanol What do you do to speed the reaction rate in both reactions? (1.5 points) Nu :
Which of the follow would you expect to react fastest with silver nitrate in ethanol? primary alkyl bromide primary alkyl chloride secondary alkyl chloride tertiary alkyl bromide
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