Homework Answers
First, about what resultswe talking about? Temperature? pressure? ph? We need some information, but anyway, the losses of a reactant causes a low conversion, if we talking about in these terms, and if we talking that the alkyl halide is a product, so, we talking about a losses of pressure in the vessel storage.
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4. How would your results be affected if some of the low boiling alkyl halide was...
6. The procedure for this lab when actually done specifies refluxing the alkyl halide with the...
6. The procedure for this lab when actually done specifies refluxing the alkyl halide with the alkoxide base in dry alcohol as the solvent. a. What substance should be missing from a dry reagent? b. Write a reaction equation, using structures, for the reaction that would occur between the substance you mentioned in part a and tert-butoxide and label the acid, base, conjugate acid, and conjugate base in the reaction. c. How would the presence of the conjugate base formed...
Experiment 4: Synthesis of a tertiary alkyl halide Page 5 of 6 Experiment 4: Synthesis of...
Experiment 4: Synthesis of a tertiary alkyl halide Page 5 of
6
Experiment 4: Synthesis of a tertiary alkyl halide Page 5 of 6 Assuming that all other experimental conditions are the same; explain if an S,1 reaction would still occur if the following changes were made. If an Sk1 reaction would still occur: then state the IUPAC name and draw the structure of the product formed compare the rate of reaction to the rate of the original reaction (in...
2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2...
2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2 mechanism? Explain your answer. Canna omaan " Lara
Indicate which alkyl halide you would expect to react more rapidly by an Si2 4 mechanism....
Indicate which alkyl halide you would expect to react more rapidly by an Si2 4 mechanism. (2 pts.) Explain your answer. (2 pts.) CI or
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 Distillation is a technique that is to purify liquid com...
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 Distillation is a technique that is to purify liquid compounds. Use theoretical data to explain how distillation is used to separate the target product in this reaction from any residual unreacted starting material in the reaction. [2 marks]
How would you carry out the synthesis below? Additional carbons may come from any alkyl halide...
How would you carry out the synthesis below? Additional
carbons may come from any alkyl halide with 3 C's or less. Show the
reagents needed for each step of your transformation, but do NOT
draw the mechanisms for each step.
SHORT ANSWER #30: How would you carry out the synthesis below. Additional carbons may come from any alkyl halide with 3 C's or less. Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms...
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 The term "side reactions"...
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 The term "side reactions" refers to any chemical reaction that can occur that form products other than the desired product. Side reactions can consume the reactants of your intended reaction, and can affect the percent yield of your target product. Draw the full reaction mechanism for a possible side reaction that can occur under these reaction conditions. Include all charges and intermediates. Vaguely directed arrows will not receive...
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary....
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
How would you carry out the synthesis below? Additional carbons may come from any alkyl halide...
How would you carry out the synthesis below? Additional carbons may come from any alkyl halide with 30's or less, Show the reagents needed for each step of your transformation, but do not draw mechanisms for each step. the -->
How would your calculated value for the molecular weight of your unknown been affected (high, low,...
How would your calculated value for the molecular weight of your unknown been affected (high, low, no effect) if a small quantity of the unknown stuck to the metal stirring rod and failed to dissolve in the benzophenone?
6. The procedure for this lab when actually done specifies refluxing the alkyl halide with the alkoxide base in dry alcohol as the solvent. a. What substance should be missing from a dry reagent? b. Write a reaction equation, using structures, for the reaction that would occur between the substance you mentioned in part a and tert-butoxide and label the acid, base, conjugate acid, and conjugate base in the reaction. c. How would the presence of the conjugate base formed...
Experiment 4: Synthesis of a tertiary alkyl halide Page 5 of
6
Experiment 4: Synthesis of a tertiary alkyl halide Page 5 of 6 Assuming that all other experimental conditions are the same; explain if an S,1 reaction would still occur if the following changes were made. If an Sk1 reaction would still occur: then state the IUPAC name and draw the structure of the product formed compare the rate of reaction to the rate of the original reaction (in...
2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2 mechanism? Explain your answer. Canna omaan " Lara
Indicate which alkyl halide you would expect to react more rapidly by an Si2 4 mechanism. (2 pts.) Explain your answer. (2 pts.) CI or
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 Distillation is a technique that is to purify liquid compounds. Use theoretical data to explain how distillation is used to separate the target product in this reaction from any residual unreacted starting material in the reaction. [2 marks]
How would you carry out the synthesis below? Additional
carbons may come from any alkyl halide with 3 C's or less. Show the
reagents needed for each step of your transformation, but do NOT
draw the mechanisms for each step.
SHORT ANSWER #30: How would you carry out the synthesis below. Additional carbons may come from any alkyl halide with 3 C's or less. Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms...
Experiment 4: Synthesis of a tertiary alkyl halide Page 3 of 6 The term "side reactions" refers to any chemical reaction that can occur that form products other than the desired product. Side reactions can consume the reactants of your intended reaction, and can affect the percent yield of your target product. Draw the full reaction mechanism for a possible side reaction that can occur under these reaction conditions. Include all charges and intermediates. Vaguely directed arrows will not receive...
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
How would you carry out the synthesis below? Additional carbons may come from any alkyl halide with 30's or less, Show the reagents needed for each step of your transformation, but do not draw mechanisms for each step. the -->
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