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"In Lecture-Practice” assignment (part 03) upload your solution to Bb “Test $ Quizzes” for credit Outline...
KU LECTURE: ALDEHYDE AND KETONES. PART 02 PREPARATION OF IMINES AND ENAMINES "In Lecture-Practice” assignment (part...
KU LECTURE: ALDEHYDE AND KETONES. PART 02 PREPARATION OF IMINES AND ENAMINES "In Lecture-Practice” assignment (part 01) upload your solution to Bb “Test $ Quizzes” for credit Draw a step-by-step mechanism and provide products for these two reactions. pH = 3-6 ? NH2 au que pH = 3-6 ?
Please answer part a) and b) to question 2 Name Student ID BOO Upload answer 2....
Please answer part a) and b) to question 2
Name Student ID BOO Upload answer 2. [10 marks] Clearly show how you could make the required products from the starting compounds that are provided. Use only reactions you have learned in CHEM 2402 or 2401. Gilman and Grignard reagents must only contain carbon and hydrogen as the reagent. Multiple reaction pathways may be equally correct. Protecting groups may be necessary. Show the reaction conditions, including temperature when important, for every...
**(left structure)****(right structure)** The two structures for the assignment are above and the task is: 1....
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
Assignment 4 provides practice with applying the ERD notation to narrative problem descriptions. This assignment involves...
Assignment 4 provides practice with applying the ERD notation to narrative problem descriptions. This assignment involves problems 20, 33, 34, 35, and 36 on Page 224 in the textbook (Chapter 6). Plan to use the drawing tool of your choice to create the ERD then copy and paste each ERD into a Word document. Label the problems in your Word document to match the problem in the textbook. Problems 33 to 36 are worth 15% each. Problem 20 is worth...
DIRECTIONS: Reflect upon the calculation lectures received during your dosage from courses, and Professional Practice III....
DIRECTIONS: Reflect upon the calculation lectures received during your dosage from courses, and Professional Practice III. Consider the following TPN medication order (Table 1) and the Stock Solutions (Table 2); then determine the exact volume of cach component that should be used to compound the preparation. Round to the nearest whole mL. Answers will be incorrect if not appropriately rounded. To receive all credit, show all work. This assignment can be typed or handwritten, but all work must be shown....
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could...
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
KU LECTURE: ALDEHYDE AND KETONES. PART 02 PREPARATION OF IMINES AND ENAMINES "In Lecture-Practice” assignment (part 01) upload your solution to Bb “Test $ Quizzes” for credit Draw a step-by-step mechanism and provide products for these two reactions. pH = 3-6 ? NH2 au que pH = 3-6 ?
Please answer part a) and b) to question 2
Name Student ID BOO Upload answer 2. [10 marks] Clearly show how you could make the required products from the starting compounds that are provided. Use only reactions you have learned in CHEM 2402 or 2401. Gilman and Grignard reagents must only contain carbon and hydrogen as the reagent. Multiple reaction pathways may be equally correct. Protecting groups may be necessary. Show the reaction conditions, including temperature when important, for every...
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
DIRECTIONS: Reflect upon the calculation lectures received during your dosage from courses, and Professional Practice III. Consider the following TPN medication order (Table 1) and the Stock Solutions (Table 2); then determine the exact volume of cach component that should be used to compound the preparation. Round to the nearest whole mL. Answers will be incorrect if not appropriately rounded. To receive all credit, show all work. This assignment can be typed or handwritten, but all work must be shown....
Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...
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