1. Calculate the theoretical amount (in mL) of CH3CH2CH2CH2CN (valeronitrile) needed to make 2.50 grams of CH3CH2CH2CH2COOH (valericacid). Show your work for each step. Note: this question is not askingabout benzonitrile, it is asking about valeronitrile. 2. Look up anastrozole in the Merck Index. If this molecule underwenthydrolysis, what would the product look like?

1. Calculate the theoretical amount (in mL) of CH3CH2CH2CH2CN (valeronitrile) needed to make 2.50 grams of CH3CH2CH2CH2COOH (valericacid). Show your work for each step. Note: this question is not askingabout benzonitrile, it is asking about valeronitrile. 2. Look up anastrozole in the Merck Index. If this molecule underwenthydrolysis, what would the product look like?

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.63P

See similar textbooks

Similar questions

Please Help
Which method (it may be multiple steps) would complete the following reaction? CH₂CH₂CH₂Br 1) CO2, 2) NaCl 1) NaCN, 2) H30* 1(LiAlH4, 2( H30* 1(LDA, 2) H,O CH₂CH₂CH₂C-OH
I need help with predicting the ester.
How do we know what 1.1 equivalents are? Would it be 1.1 mmol? Same with 1 equivalent, 2.5 equivalents
Make sure you label everything as labeled as asked and make sure you explain everything is asked step by step.
Another extraction procedure involves extracting the acid first. Fill in the following flowchart before the start of your lab session. Show the completed flowchart to the TA as you enter the lab; this is part of your writeup. Ether solution Ether layer Aqueous layer Aqueous layer OH Benzoic acid 1. Add 3 M HCI 2. Separate the layers Add 6 M NaOH H₂N- Ethyl 4-aminobenzoate 1. Add 3 M NaOH 2. Separate the layers Aqueous layer OCH₂CH3 Aqueous layer Add 6 M HCI
Sample Qualitative test (Observation) Chromic acid Test Lucas Test lodoform Test 1-butanol Oxidation occurred. Turbidity did not No reaction Occur 2-butanol Oxidation occurred. Turbidity occurred. Jurbidityoccurred Reaction occurred. 2-methyl-propanol Oxidation did not Reaction occurred. occur. General Equations and Purpose of the Test Chromic acid Test: ntion
Match column A (common active ingredients of insect repellants) to column B (IUPAC names). Column A Column B 1. Citronellol and Geraniol a. 6 parts DMP, 2 parts Indalone, and 2 part of Rutgers 612 b. Six esters (pyrethrins) 2. DEET 3. DMP c. 1-piperidine carboxylic acid-2(2- 4. 6-2-2 hydroxyethyl)-1-methylpropyl ester d. 3-(N-acetyl-N-butyl) aminopropionic acid 5. Picaridin 6. Citriodiol ethyl ester 7. IR-3535 e. butyl-3,3- dihydro-2,2-dimethyl-4-oxo-2H- pyran-6-carboохуlate f. para-menthane-3,8-diol 8. Rutgers 612 9. Indalone g. dimethyl phthalate 10. Pyrethrum h. 2-ethyl-1,3-hexanediol i. 3,7-Dimethyloct-6-en-1-ol j. N, N-diethyl-m-toluamide
What are the reagents and chemical groups
Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product.
Can you help me draw both the intramolecular and intermolecular Gringnard reactions?
10) Dr. Rashmi uses a rather specific three-steps procedure (described below) to cook up a spicy sugar derivative. Why does she make use of such a protocol? Describe the purpose of each steps. 1) acetone, cat. H* 2) 2,5-dimethylbenzyl bromide, NaH 3) H30*, r.t. он NH2 "NH2 'Buo "Buo ´OBu O'Bu