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Which direction does the equilibrium of the following reaction? ALSO chose a term that best explains...
NaNH2 H2O --> NaOH NH3 Which direction does the equilibrium of the following reaction? ALSO chose...
NaNH2 H2O --> NaOH NH3 Which direction does the equilibrium of the following reaction? ALSO chose a term that best explains why you chose that answer. Reaction favors Left Side of Equation Reaction favors Right Side of Equation Electronegativity Resonance Size of electron cloud Inductive Effect
need help with all problems listed Uuuuuuuuu 34. (D4) The fol The following reaction produced only...
need help with all problems listed
Uuuuuuuuu 34. (D4) The fol The following reaction produced only one product. The DESIRED product was not ed. What molecule was produced? How would you synthesize the desired product heginning with the SAME starting material? produced. Wb AICI: DESIRED Product (Not Produced) Isolated Product Hint: C10H14 27. (D4) Why does Why does reaction A produce a mixture of products when reaction B produces a Le regioisomer? Provide mechanisms for both reactions. Br OH NaOH...
11. Which of the following best explains why the synthetic route shown below would be unsuccessful?...
11. Which of the following best explains why the synthetic route shown below would be unsuccessful? 2) NaNH2 3) (CHs)hCBr A) The alkynide anion is not a strong enough nucleophile to react with 1-bromopropane in step 1 m amide is not a strong enough base to deprotonate the terminal alkyne in step anion formed by reaction with sodium amide will facilitate an E2 (rather C) The alkynide than SN2) reaction with t-butyl bromide. 5oth substtution reactions will occur on the...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
Question 1 The following reaction between 2-methylbut-2-ene and hydrogen bromide (HBr) is best described as what...
Question 1 The following reaction between 2-methylbut-2-ene and hydrogen bromide (HBr) is best described as what type of reaction? Refer to the Figure A) Addition B) Substitution C) Elimination D) Rearrangement Question 2 For the reaction in question 1, two products are possible- a major product, and a minor product. For the minor product, what is the splitting pattern for the added hydrogen (highlighted in red) that would be observed in the molecules HINMR spectrum? Refer to the Figure HBr...
Part I Color changes of Methyl Violet. We will study the following reaction: HMV (aq) +...
Part I Color changes of Methyl Violet. We will study the following reaction: HMV (aq) + MV (aq) + H* (aq) yellow greenish-blue violet Step 1. Place about 4 mL of distilled water in a regular test tube. Add two drops of methyl violet indicator. Record the color of the solution. Violet Next, add drop by drop, add 6M HCI. This forces equilibrium to be shifted to the left or right-circle the right answer). Adding HCl changes color from to...
need help with all problems listed
Uuuuuuuuu 34. (D4) The fol The following reaction produced only one product. The DESIRED product was not ed. What molecule was produced? How would you synthesize the desired product heginning with the SAME starting material? produced. Wb AICI: DESIRED Product (Not Produced) Isolated Product Hint: C10H14 27. (D4) Why does Why does reaction A produce a mixture of products when reaction B produces a Le regioisomer? Provide mechanisms for both reactions. Br OH NaOH...
11. Which of the following best explains why the synthetic route shown below would be unsuccessful? 2) NaNH2 3) (CHs)hCBr A) The alkynide anion is not a strong enough nucleophile to react with 1-bromopropane in step 1 m amide is not a strong enough base to deprotonate the terminal alkyne in step anion formed by reaction with sodium amide will facilitate an E2 (rather C) The alkynide than SN2) reaction with t-butyl bromide. 5oth substtution reactions will occur on the...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
Question 1 The following reaction between 2-methylbut-2-ene and hydrogen bromide (HBr) is best described as what type of reaction? Refer to the Figure A) Addition B) Substitution C) Elimination D) Rearrangement Question 2 For the reaction in question 1, two products are possible- a major product, and a minor product. For the minor product, what is the splitting pattern for the added hydrogen (highlighted in red) that would be observed in the molecules HINMR spectrum? Refer to the Figure HBr...
Part I Color changes of Methyl Violet. We will study the following reaction: HMV (aq) + MV (aq) + H* (aq) yellow greenish-blue violet Step 1. Place about 4 mL of distilled water in a regular test tube. Add two drops of methyl violet indicator. Record the color of the solution. Violet Next, add drop by drop, add 6M HCI. This forces equilibrium to be shifted to the left or right-circle the right answer). Adding HCl changes color from to...
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