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Ch. 10 Homework Organic Chemistry ! - Fall 2019 Name: Due Date: 11/20/19 1. (7 pts)...
Organic Chem Ch 11 worksheet Name Homework #7 20 Points Due 11/20/19 1) Name the following...
Organic Chem Ch 11 worksheet
Name Homework #7 20 Points Due 11/20/19 1) Name the following (6 points) NH2 он 2) Draw the following (4 points) (1R)-1-bromo-N-methylpentan-1-amine (2R)-2-cyanopropanoic acid 3) What are the products and mechanisms for both products? (4 points) HBr Thermodynamic Kinetic 4) Fill-in the Boxes (6 points) НCL Br Only Products Br 1) LDA (2X) 2) H2SO4, HgSO, H20 НВr, -80°C One Product
Advanced Organic Chemistry Homework Due 11-1-19 Show the products or reactants of the following Diels-Alder reactions....
Advanced Organic Chemistry Homework Due 11-1-19 Show the products or reactants of the following Diels-Alder reactions. INTRA Molecular Me Мео доме OME DIELS - IL
What is the major organic product for #2,4,5? On the synthesis what is the reagents, starting...
What is the major organic product for #2,4,5?
On the synthesis what is the reagents, starting materials, and
intermediates?
the major organic product(s) of the following reactions. Indicate stereochemistry Reactions, Predict Where neAnswer 4 reactions below, 1 points each, 4 points total). bold and dashed wedges). Partial credit will be given to correct work so show 1. Excess CHal 3. Heat necessary (with NH2 1. NaNO2. HC 2. CuCN 2. Br 2. H2N-NH2 (CH3)2CHOH 1. PhCH2NH2 2. LiAIHA 5. Synthesis....
Chapter 9 Organic Chemistry 1 Homework 7. Starting with ethyne, outline syntheses of each of the...
Chapter 9 Organic Chemistry 1 Homework 7. Starting with ethyne, outline syntheses of each of the following. other needed reagents, and you need not show the synthesis of compounds prep carlier parts of this problem. (a) Propyne, (b) 1-Butyne, (c) 2-Butyne, (d) cis-2-Butene (e) trans-2-Butene (1) 1-Pentyne, (s) 2-Hexyne, (h) (Z)-2-Hexene (E )-2-Hexene, () 3-Hexyne, (k) ó b 8. Write structures for the maior arcanic products from the following reactions. Show stereoisomers where applicable. (c) (1) Na CL, (1 equiv.)...
Homework Problem Set 8 Iverson CH320M/328M Due Friday. Nov. 9 7. The point of organic chemistry...
Homework Problem Set 8 Iverson CH320M/328M Due Friday. Nov. 9 7. The point of organic chemistry is synthesis, the conversion of starting molecules into different ones with a new structure and function. Each reaction you are learning should be thought of as a "tool" that allows you to create a desired type of molecule combinations to create truly interesting molecules. In the large boxes provided, draw the structures of the molecules Indicated In this synthesis scheme. For smaller boxes next...
Ochem 2 ch 22 Ch 22 Amines (100 pts) Chemistry 2320 7. Provide an efficient multi-step...
Ochem 2 ch 22
Ch 22 Amines (100 pts) Chemistry 2320 7. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents used for each step by writing them over the arrow leading to each of the specified products. At some point in your synthesis you must utilize arrows. chemical(s) specified over the OH 2 8. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents...
Ochem 2 ch 19-20 Chemistry 2320 Ch 19 and 20-Carboxylic Acids and Derivatives (100 pts) Select...
Ochem 2 ch 19-20
Chemistry 2320 Ch 19 and 20-Carboxylic Acids and Derivatives (100 pts) Select the products and the reagents for the following sequence by writing the numbers of the products formed in the box and the letter of the reagents used over the arrows. The order of steps is important. Not all products or reagents will be used. 4. A. CH OH, H2SO, (cat) Number: OH Letter B. Na Cr O H2SO C. Br CO-CH C D. O...
CH 110 General, Organic, & Biological Chemistry: Fall 2019 pter 7 Hem 7.42 - Enhanced -...
CH 110 General, Organic, & Biological Chemistry: Fall 2019 pter 7 Hem 7.42 - Enhanced - with Feedback Classify each of the following as a combination, decomposition, single replacement, double replacement, or combustion reaction Sort these reactions into the proper categories AgNO3(aq) aCl(aq) AgCl(s) + NaNO3(aq) 2AgBr(s)- 2Ag(s) + Br() 2CH.(1) + 150 (8) 12C02(g) + 6H2O(g) Zn(s) + CuCl(aq) -- Cu(s) + ZnCl(aq) 3H2(g) + N2(g) + 2NH3(g) Combination Decomposition Single replacement Double replacement Combustion Seet 2- Enhanced -...
IT IS AN ORGANIC CHEMISTRY SYNTHESIS QUESTION 6. Synthesis: (40 pts) Show how you would carry...
IT IS AN ORGANIC CHEMISTRY SYNTHESIS QUESTION
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI The product should be 3-chloro-3-methylhexane A) Cyclobutane 1) 2) 1) 2) como B) OH 1) 2)
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where...
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where necessary (4 points SOCIE нанд tok OMSO HCI (2 e) 2 SYNTHESIS: How would you prepare compound 1 from cyclopentanol? You may use any other organic reagents of inorganic reagents you wish but you must start with cyclopentanol. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate and products of each synthetic step but NO MECHANISMS....
Organic Chem Ch 11 worksheet
Name Homework #7 20 Points Due 11/20/19 1) Name the following (6 points) NH2 он 2) Draw the following (4 points) (1R)-1-bromo-N-methylpentan-1-amine (2R)-2-cyanopropanoic acid 3) What are the products and mechanisms for both products? (4 points) HBr Thermodynamic Kinetic 4) Fill-in the Boxes (6 points) НCL Br Only Products Br 1) LDA (2X) 2) H2SO4, HgSO, H20 НВr, -80°C One Product
Advanced Organic Chemistry Homework Due 11-1-19 Show the products or reactants of the following Diels-Alder reactions. INTRA Molecular Me Мео доме OME DIELS - IL
What is the major organic product for #2,4,5?
On the synthesis what is the reagents, starting materials, and
intermediates?
the major organic product(s) of the following reactions. Indicate stereochemistry Reactions, Predict Where neAnswer 4 reactions below, 1 points each, 4 points total). bold and dashed wedges). Partial credit will be given to correct work so show 1. Excess CHal 3. Heat necessary (with NH2 1. NaNO2. HC 2. CuCN 2. Br 2. H2N-NH2 (CH3)2CHOH 1. PhCH2NH2 2. LiAIHA 5. Synthesis....
Chapter 9 Organic Chemistry 1 Homework 7. Starting with ethyne, outline syntheses of each of the following. other needed reagents, and you need not show the synthesis of compounds prep carlier parts of this problem. (a) Propyne, (b) 1-Butyne, (c) 2-Butyne, (d) cis-2-Butene (e) trans-2-Butene (1) 1-Pentyne, (s) 2-Hexyne, (h) (Z)-2-Hexene (E )-2-Hexene, () 3-Hexyne, (k) ó b 8. Write structures for the maior arcanic products from the following reactions. Show stereoisomers where applicable. (c) (1) Na CL, (1 equiv.)...
Homework Problem Set 8 Iverson CH320M/328M Due Friday. Nov. 9 7. The point of organic chemistry is synthesis, the conversion of starting molecules into different ones with a new structure and function. Each reaction you are learning should be thought of as a "tool" that allows you to create a desired type of molecule combinations to create truly interesting molecules. In the large boxes provided, draw the structures of the molecules Indicated In this synthesis scheme. For smaller boxes next...
Ochem 2 ch 22
Ch 22 Amines (100 pts) Chemistry 2320 7. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents used for each step by writing them over the arrow leading to each of the specified products. At some point in your synthesis you must utilize arrows. chemical(s) specified over the OH 2 8. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents...
Ochem 2 ch 19-20
Chemistry 2320 Ch 19 and 20-Carboxylic Acids and Derivatives (100 pts) Select the products and the reagents for the following sequence by writing the numbers of the products formed in the box and the letter of the reagents used over the arrows. The order of steps is important. Not all products or reagents will be used. 4. A. CH OH, H2SO, (cat) Number: OH Letter B. Na Cr O H2SO C. Br CO-CH C D. O...
CH 110 General, Organic, & Biological Chemistry: Fall 2019 pter 7 Hem 7.42 - Enhanced - with Feedback Classify each of the following as a combination, decomposition, single replacement, double replacement, or combustion reaction Sort these reactions into the proper categories AgNO3(aq) aCl(aq) AgCl(s) + NaNO3(aq) 2AgBr(s)- 2Ag(s) + Br() 2CH.(1) + 150 (8) 12C02(g) + 6H2O(g) Zn(s) + CuCl(aq) -- Cu(s) + ZnCl(aq) 3H2(g) + N2(g) + 2NH3(g) Combination Decomposition Single replacement Double replacement Combustion Seet 2- Enhanced -...
IT IS AN ORGANIC CHEMISTRY SYNTHESIS QUESTION
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI The product should be 3-chloro-3-methylhexane A) Cyclobutane 1) 2) 1) 2) como B) OH 1) 2)
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where necessary (4 points SOCIE нанд tok OMSO HCI (2 e) 2 SYNTHESIS: How would you prepare compound 1 from cyclopentanol? You may use any other organic reagents of inorganic reagents you wish but you must start with cyclopentanol. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate and products of each synthetic step but NO MECHANISMS....
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