Post Lab QuestionsWilliamson Éther Synthesis**Draw structures in your answers, just a name or formula will not suffice**1. What would have been the effect of using-a. Ethyl iodide instead of ethyl bromide-b. 2 bromopropane instead of ethyl bromidec. Bromobenzene instead of ethyl bromide.d. NaH instead of NaOH

a. Ethyl iodide instead of ethyl bromide:Using ethyl iodide instead of ethyl bromide would likely…

Answered: Post Lab Questions Williamson Éther…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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label and provide PRIORITY SCALE FOR NOMENCLATURE
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Which of the follow reactions would produce a primary alcohol? Drag and drop options on the right- hand side to reorder and match with items on the left. Reordering may cause items on the right-hand side to swap positions. 1. Yes 2. Yes No No No No 1) NABH, CH,OH 2) 1. LIAIH,, ether 2. H,0 3) 1. excess LIAIH,, ether 2. Н,о 4) NABH, CH,OH он II II II 3. 4.
Which of the following is NOT a good starting material for the synthesis of 2-pentanol? A. 2-bromopentane B. 2-pentanone C. 2-pentene D. 1-pentene
Which of the below do you think would have the highest boiling point? Why? a. butane b. butanal C. 2-butanol d. butanoic acid d speaker notes Explores
The synthesis of cyclohexanone oxime from cyclohexanone is a net? a. elimination b. substitution C. addition d. rearrangement The synthesis of cyclohexanone oxime from cyclohexanone is a net of carbon? a. reduction b. oxidation C. not a redox of carbon Balancing the equation of all the starting reagents going to final products in the synthesis of cyclohexanone oxime from cyclohexanone (see the first question), what is the coefficient of water if the coefficient of cyclohexanone is one? Give your answer in decimal form with no units. Answer: Select all the effects that you should see in an infrared going from cyclohexanone to cyclohexanone oxime. Selecting wrong answers may give you a negative score. a. a peak should disappear from above 3000 cm -1 b. a new peak should appear above 3000 cm -1 c. the frequency of the infrared absorption should go down in the double bond region d. the frequency of the infrared absorption should go up in the double bond region
Predict and name the product. 1. NaNH2 2. Br A. 2-methyl-3-hexyne B. 2-methyl-3-heptyne C. 2-methyl-4-heptyne D. 6-bromo-3-hexyne E. 7-bromo-2-methyl-3-heptyne
Organic 2 help. (Not used hend raiting)
36. Assign the IUPAC name of the structure below. A. 1-Bromopentan-3-one B. 3-Bromocyclopentanone C. 3-bromocylopentanal D. Both B and C 37. Assign the IUPAC name of the structure below. (Hint: Check the order of precedence) H A. Pentan-1,4-dione B. 1,4-Pentanaldehyde C. 4-Oxopentanal D. None of the above 38. Assign the IUPAC name of the structure below. (Hint: Check the order of precedence) A. 4-hydroxy-3-methylcyclohexanone B. 2-Methyl-4-oxophenol C. 2-Methyl-3-hydroxycylohexanone D. 4-phenyl-2-methylhexanone
Hello, I do not understand these questions for chemistry and I am stuck. May I get help please please?? An explanation leading to steps would be helpful. Thank you. Question: Draw the MAJOR organic product(s) for the following reactions. If no reaction occurs, state ‘no reaction’ in the box provided.
For the reaction conditions given below, what type of product will be produced? Ketone + Zn(Hg) +HCl ——-> A. an alcohol B. an alkane C. an aldehyde D. a ketone E. no reaction will occur
What is the IUPAC name for this compound? Select one: a. 1,4-dimethyl-2-cyclohexanone b. cyclohexyl methyl ketone c. 2,5-dimethylcyclohexanone d. methylcyclohexanone e. 1,4-dimethyl-3-cyclohexanone

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