1.Heat
20 mL of water in a 250 mL beaker to the boiling point using a hot
plate. DO NOT use the bunsen burner as there are flammable alcohol
being used openly in the lab.
2.While the water is heating prepare a clean dry large test
tube.
3.In the test tube place 10 mL of one of the alcohol and 10 mL of
one of the acids. Set this aside.
4.Using a dropper pipette get some concentrated sulphuric acid.
CAUTION: concentrated sulphuric acid is extremely corrosive to skin
and clothing.
5.Place the large test tube in the boiling water. Add 10 drops of
the sulphuric acid to the alcohol, carboxylic acid mixture in the
test tube.
6.Boil the reaction for 5 minutes.
7.To a clean distilling flask, add 50 mL of distilled water and the
contents of your large test tube.
8.Set up your distilling apparatus and distill the ester from the
distillation flask mixture. It should be the first substance that
comes off. Record the temperatures every 30 seconds after the
temperature of the mixture starts to climb quickly.
9.Your ester is the distillate. Packing the outside of the
receiving flask with ice will help condense your ester.
Write out the full mechanism (with arrows) for the formation of Pentyl Propionate. And explain what...
Draw mechanism of the pictured reaction. 6. Write out a reasonable mechanism to show how your acid catalyst (diphenylphosphoric aciod, represented below by H-A) and 1,4-benzene dimethanol react with with &-decalactone in the following reaction. (NOTE: this happens on the other side benzenedimethanol, and keeps happening on the groups every time a monomer is added). OH OH H-A catalyst HO
2. Using curved arrows to symbolize the flow of electrons, write the stepwise mechanism for the condensation reaction between decandioyl dichloride and 1,6-hexanediamine. 3. Write an equation for the formation of the salt produced from one molecule of hexanedioic acid and two molecules of 1,6-hexanediamine. 4. Why is sodium carbonate used in the reaction to prepare Nylon-6,10? 5. There is a large decrease in the bulk of the rope of Nylon-6,10 upon drying. Explain this observation. 6. Using full structural...
please do all and explain sn1 sn2 e1e2 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
Write out a mechanism for any reaction mechanism involving at least two steps. Include electron-pushing arrows, lone pairs and formal charges.
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CONCEPT QUESTIONS Mechanism. While the reaction carried out in lab used potassium hydroxide as the catalyst, many other catalysts have been developed to increase regioselectivity and stereoselectivity in aldol condensations. One small molecule catalyst commonly used is proline, a naturally occurring amino acid. The mechanism involves the initial formation of an enamine; predict the structure of this enamine intermediate (intermediate A), and draw the mechanism for the conversion of intermediate A to intermediate B. Helpful Hint: The formation of the...
Add arrows to the boxes to show the mechanism of the formation of the thermodynamic product of the reaction. All charges, necessary lone pairs, bonds are shown, so you only have to provide the curved arrows to convert a structure to the one in the following box. In the last box, draw the thermodynamic product of the reaction. Include any necessary lone pairs in your structure. **only the second & fourth box is wrong ** please help and explain why....
Write out the complete mechanism for the Fischer esterification using curved arrows. What does the symbol mean in the reaction?
Please explain and right in details 145 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: NaOCH, Br a) H2O2 - b) NaOH 0-s- 4.5 'o:
Mechanism. While the reaction carried out in lab used potassium hydroxide as the catalyst, many other catalysts have been developed to increase regioselectivity and stereoselectivity in aldol condensations. One small molecule catalyst commonly used is proline, a naturally occurring amino acid The mechanism involves the initial formation of an enamine; predict the structure of this enamine intermediate (intermediate A), and draw the mechanism for the conversion of intermediate A to а. intermediate B. Helpful Hint: The formation of the new...