Homework Answers
Step 1: base catalyzed: 4
Step 2: base catalyzed: 1
Step 3: base catalyzed: 6
Step 1: acid catalyzed: 2
Step 2: acid catalyzed: 5
Step 3: acid catalyzed:3
Add Answer to:
Your answer is partially correct. Try again For the reaction shown in Box 11-1 (the attack...
Question 17 Predict the major product(s) for the reaction shown below. (choose all correct answers) Br2...
Question 17 Predict the major product(s) for the reaction shown below. (choose all correct answers) Br2 ?? Br Br Br Br Br Br Br பி Question 18 Which of the reaction steps, shown below, would be part of the mechanism for the acid-catalyzed hydration of trans-but-2-ene? (choose all correct answers) OH но н-о-s-он + H нн H-O-S-OH Он + о H H онн нн :Он он H H нн O нн H-O-S-OH он + OH o=S-O
Could you please help me with these? Thank you!!! Your answer is partially correct. Try again....
Could you please help me with
these?
Thank you!!!
Your answer is partially correct. Try again. (a) он Alkyl iodide Edit Н,С Nucleophile: Он Edit c) CN Alkyl iodide: Н.С Н,С. Ш/ Edit Nucleophile: н.с— NH2 Edit
Jame: . Complete this mechanism for the following substitution reaction. Note: this reaction is balanced. H-Br...
Jame: . Complete this mechanism for the following substitution reaction. Note: this reaction is balanced. H-Br Н,0 OH -CH3 H20 Step 1: proton transfer Step 2: lose water Step 3: attack the carbocation Br -CH3 . Each reaction above is reversible. In question 1, what effect would adding more HBr have on the equilibrium? Would there be more or less alkyl bromide product present at equilibrium? . Two dehydrations can occur on glycerol, the principle carrier molecule in vaping devices....
Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown ...
Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown below? Assume that liquid ammonia and enough HCI to make sufficient NH4 ion are present in the reaction mixture. Select all that apply. n The collapse of the tetrahedral intermediate represented by step 3 is incorrect because under the acid-catalyzed conditions, hydroxide ion will not be a viable leaving group. Leaving aside the issue of whether hydroxide ion would be present or not, the electron...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would be the absorption peak of a carbonyl, C-0, stretching in IR? a) around 3300 cm b) around 2980 cm" c) around 1700 cm d) around 1200 cm 2. What is the Grignard reagent in nucleophilic addition reaction considered? a) b) 0 c) H d) all the above 3. What a cynaohydrin contains? a) CN and NH. b) N, and OH. c) CN and OH....
Your answer is partially correct. Try again. Using the reagents below, list in order (by letter,...
Your answer is partially correct. Try again. Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis. Note: Not all spaces provided may be needed. Hints: First receive a Grignard reagent in steps 1 and 2. Use propanol in step 5. In step 9 a product from step 4 reacts with a product from step 8. a. NH3 b. Mg/ether C. SOCI2 d. 1. CO2 2. H30+ e. Na2Cr207/H2SO4/H20 f. product from step...
P10.049 Your answer is partially correct. Try again. For the beams and loadings shown, determine the...
P10.049 Your answer is partially correct. Try again. For the beams and loadings shown, determine the beam deflection at point H. Assume that EI = 9.5 x 104 kN-m2 is constant for each beanm
please circle answer Shown below is the reaction between a nitrile and a Grignard reagent. What...
please circle answer
Shown below is the reaction between a nitrile and a Grignard reagent. What would be the first step in the mechanism? CN - 1. CH3MgBr 2. H307 Nucleophile attacks nitrile carbon Hydrolysis of the nitrile Protonate the nitrile nitrogen Base Beprotonates the alpha-carbon An unknown compound shows an infrared absorption around 2250 cm (medium intensity). What structural fragment could be causing this absorption? carbonyl OOH nitrile N-H NH 1. (CH3)2CHCOCI, pyridine 2. LIAIH4 3. H2O Product tertiary...
Chapter 27, Problem 023 Partially correct answer. Your answer is partially correct. Try again. In the...
Chapter 27, Problem 023
Partially correct answer. Your answer is partially correct. Try
again. In the figure R1 = 130 Ω, R2 = 50 Ω, and the ideal batteries
have emfs ε1 = 6.0 V, ε2 = 5.0 V, and ε3 = 4.0 V. Find (a) the
current in R1, (b) the current in R2, and (c) the potential
difference between points a and b.
R2 8 R w
Give the names of each organic families shown. (Careful with spelling) My answers are partially correct...
Give the names of each organic families shown. (Careful with
spelling)
My answers are partially correct please tell me all the right
anaswers
Give the names of each organic families shown. Careful with spelling) O=O solo con modulelos.com.br CH,CH,CH; CH,CH,CH; CH,CH,CH; | CHỊCH C-O-C- CHỊCH, CHỊCH - NH Он Br ос,н. Compound I is a(n) amide Compound II is a(n) carboxylic acid Compound III is a(n) aldehyde Compound IV is a(n) alcohol Compound V is a(n) ester Submit >
Question 17 Predict the major product(s) for the reaction shown below. (choose all correct answers) Br2 ?? Br Br Br Br Br Br Br பி Question 18 Which of the reaction steps, shown below, would be part of the mechanism for the acid-catalyzed hydration of trans-but-2-ene? (choose all correct answers) OH но н-о-s-он + H нн H-O-S-OH Он + о H H онн нн :Он он H H нн O нн H-O-S-OH он + OH o=S-O
Could you please help me with
these?
Thank you!!!
Your answer is partially correct. Try again. (a) он Alkyl iodide Edit Н,С Nucleophile: Он Edit c) CN Alkyl iodide: Н.С Н,С. Ш/ Edit Nucleophile: н.с— NH2 Edit
Jame: . Complete this mechanism for the following substitution reaction. Note: this reaction is balanced. H-Br Н,0 OH -CH3 H20 Step 1: proton transfer Step 2: lose water Step 3: attack the carbocation Br -CH3 . Each reaction above is reversible. In question 1, what effect would adding more HBr have on the equilibrium? Would there be more or less alkyl bromide product present at equilibrium? . Two dehydrations can occur on glycerol, the principle carrier molecule in vaping devices....
Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown below? Assume that liquid ammonia and enough HCI to make sufficient NH4 ion are present in the reaction mixture. Select all that apply. n The collapse of the tetrahedral intermediate represented by step 3 is incorrect because under the acid-catalyzed conditions, hydroxide ion will not be a viable leaving group. Leaving aside the issue of whether hydroxide ion would be present or not, the electron...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would be the absorption peak of a carbonyl, C-0, stretching in IR? a) around 3300 cm b) around 2980 cm" c) around 1700 cm d) around 1200 cm 2. What is the Grignard reagent in nucleophilic addition reaction considered? a) b) 0 c) H d) all the above 3. What a cynaohydrin contains? a) CN and NH. b) N, and OH. c) CN and OH....
Your answer is partially correct. Try again. Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis. Note: Not all spaces provided may be needed. Hints: First receive a Grignard reagent in steps 1 and 2. Use propanol in step 5. In step 9 a product from step 4 reacts with a product from step 8. a. NH3 b. Mg/ether C. SOCI2 d. 1. CO2 2. H30+ e. Na2Cr207/H2SO4/H20 f. product from step...
P10.049 Your answer is partially correct. Try again. For the beams and loadings shown, determine the beam deflection at point H. Assume that EI = 9.5 x 104 kN-m2 is constant for each beanm
please circle answer
Shown below is the reaction between a nitrile and a Grignard reagent. What would be the first step in the mechanism? CN - 1. CH3MgBr 2. H307 Nucleophile attacks nitrile carbon Hydrolysis of the nitrile Protonate the nitrile nitrogen Base Beprotonates the alpha-carbon An unknown compound shows an infrared absorption around 2250 cm (medium intensity). What structural fragment could be causing this absorption? carbonyl OOH nitrile N-H NH 1. (CH3)2CHCOCI, pyridine 2. LIAIH4 3. H2O Product tertiary...
Chapter 27, Problem 023
Partially correct answer. Your answer is partially correct. Try
again. In the figure R1 = 130 Ω, R2 = 50 Ω, and the ideal batteries
have emfs ε1 = 6.0 V, ε2 = 5.0 V, and ε3 = 4.0 V. Find (a) the
current in R1, (b) the current in R2, and (c) the potential
difference between points a and b.
R2 8 R w
Give the names of each organic families shown. (Careful with
spelling)
My answers are partially correct please tell me all the right
anaswers
Give the names of each organic families shown. Careful with spelling) O=O solo con modulelos.com.br CH,CH,CH; CH,CH,CH; CH,CH,CH; | CHỊCH C-O-C- CHỊCH, CHỊCH - NH Он Br ос,н. Compound I is a(n) amide Compound II is a(n) carboxylic acid Compound III is a(n) aldehyde Compound IV is a(n) alcohol Compound V is a(n) ester Submit >
Most questions answered within 3 hours.
-
A marketing executive who knowingly authorizes a shoddy
defective product to be brought to market is...
asked 2 minutes ago -
Write a psudocode:
1. Define a function called authorize that takes in 2 strings,
uName, and...
asked 7 minutes ago -
What Hall voltage (in mV) is produced by a 0.180 T field applied
across a 2.60...
asked 6 minutes ago -
What mass of ethylene glycol (C2H6O2) must be added to 211.0 g
of water to obtain...
asked 8 minutes ago -
Mary's employer has a defined benefits retirement plan, which
pay 3.2% of her last year's salary...
asked 12 minutes ago -
What are the characteristics and behavior of an ethical
manager?
Explain, in your words, what ethics...
asked 28 minutes ago -
1. Which of the following is NOT an argument that McMahan uses
to show that jus...
asked 50 minutes ago -
A crate slides up a frictionless slope. At the end of 3 seconds
its velocity is...
asked 1 hour ago -
Use the following information to answer the next seven
questions.
Suppose there are three potential states...
asked 1 hour ago -
If we only have interstitial and substitutional diffusion, then
what do we consider the process of...
asked 1 hour ago -
You look at yourself in a shiny 9.6-cm-diameter Christmas tree
ball.
If your face is 21.0...
asked 1 hour ago -
If we were to measure the relaxation time of a muscle after
undergoing tetanus compared to...
asked 1 hour ago