2. I did not quite get to it, but organometallic reagents can react with other functional groups beyond carbonyls. One significant example is epoxides. Given that they are strong nucleophiles, what do you think would be the product of the following reaction. 3. And then synthesis. Outline how you could covert the given ester to the given tertiary alcohol. Note that you may have to look at chapter 17 for a review of some older reactions if you do not remember them. OH ठ from

2. I did not quite get to it, but organometallic reagents can react with other functional groups beyond carbonyls. One significant example is epoxides. Given that they are strong nucleophiles, what do you think would be the product of the following reaction. 3. And then synthesis. Outline how you could covert the given ester to the given tertiary alcohol. Note that you may have to look at chapter 17 for a review of some older reactions if you do not remember them. OH ठ from

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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[References] What carbonyl compounds might you start with in a Grignard synthesis of the following compound? 3-phenyl-3-pentanol • You do not have to consider stereochemistry. • If more than one structure fits the description, draw them all. There may be up to three carbonyl compounds that could be used. Any ester used should be a methyl ester. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. 98 TAY ? √n [ 0 + 985 / √nt ? ChemDoodle +v ChemDoodle
The following molecule can be synthesized from an epoxide and alkyllithium reagent, followed by aqueous workup. However, there are two ways in which this molecule can be formed. In one approach, the epoxide has a higher molecular weight than the epoxide used in the other approach. Draw both versions in the boxes below. Draw the carbon-lithium bond as a covalent bond. Part 1:Draw the combination of epoxide and alkyllithium reagent that uses a lower molecular weight epoxide. Part 2: Draw the combination of epoxide and alkyllithium reagent that uses a higher molecular weight epoxide.
5. Synthesis Design a synthesis of the following transformation. Show how the following multi-step chemical transformation can take place. Provide reagents for each step in the synthesis. Include structures of intermediate products. Do not provide a mechanism or curved arrows. Be neat and clear! Note any special instructions. Clearly label each step in the transformation.. ? OH
Direction: predict the major new product if any resulting from the each of the following reactions please use this example as example. Dont use the stick form those are confusing.
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[References] How would you synthesize the following compounds from butanenitrile using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Example: ab Reagents 1. NaOH / H2O 2. H3O* SOCI2 1. NABH4 a e i 2. H3O* 1. ВНз / THF 2. НаО2/ NaOН b f 1. LIAIH4 1. CH3CH2MGBR / dry ether 2. H30* j 2. H3O* 1. (CH3)2CHMGB / dry ether 2. H30* PBR3 g NaCN k d Dess-Martin h CrO3 / H30* conc. HCI periodinane in CH2CI2 a) 2-Methyl-3-hexanone b) Pentanoic acid
use any reagent the reagent below just examples!!!
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Starting with ACETYLENE as your ONLY source of carbons synthesize the following compound. You may use any other inorganic reagent we have learned but any Grignard reagent must be made! You must use at least 1 new reaction from the Chapter 14: Organometallics and 1 new reaction from Chapter 15: Alcohols, Diols, Thiols notes! jual
In the reactions below, there is a main reaction step followed by one or more workup steps (which are bold-faced). Briefly explain the purpose of the bold-faced workup step in both cases, based on your experience carrying out this reaction (or a similar reaction) in the lab. (MTBE= methyl tert-butyl ether) By means of an equation explain briefly what the purpose of step 2 in the work-up (shown in boldface) was in the synthesis of aspirin.
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