Homework Answers
Solution :
4) The reaction of 2-methyl pentameter with Br2 results into the formation of five products. These five products (A to E) are given below.
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Question 4& 5
4. What are the mono-halogenated products, including stereo and constitutional isomers, from the...
1. Draw all constitutional isomers formed in the elimination reaction and predict the major product using...
1. Draw all constitutional isomers formed in the elimination reaction and predict the major product using the Zaitsev rule. A . KOCICH ! KOC(CH) 2. Draw all possible elimination reaction product(s) for the following alkyl halide. 4. Classify the following alkenes as mono, di-, tri, or tetra- substituted alkenes. Then, circle the most stable one. thayo by my 5. Which of the following alkenes is more stable?
QUESTION 4 What is the relationship between the following molecules? Br Br Br Identical Constitutional Isomers...
QUESTION 4 What is the relationship between the following molecules? Br Br Br Identical Constitutional Isomers Diastereomers Enantiomers No relationship QUESTION 5 What is the relationship between the following molecules?
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using...
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
write the structures for all the alkene products that could resonably be formed from each of...
write the structures for all the alkene products that could
resonably be formed from each of the following compounds under yhe
indicated reaction.
4. Write the structures for all the alkene products (regio and stereo isomers) that could reasonably be formed from each of the following compounds under the indicated reaction conditions. Where more than one alkene is produced, specify the one that is the major product. (5) a. 3-Methyl-3-pentanol (sulfuric acid, 80°C) b. 2,3-Dimethyl-2-butanol (phosphoric acid, 120°C)
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label...
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label the mechanism as E2 or E1. a. 2-bromo butane reacts with methoxide b. 1-chloro-1-ethyl 2 methyl cyclopentane reacts with water 2. For which reaction mechanism are each of the following statements true? Mechanism S1, S2, E1 or E2. A statement may be true for one or more mechanisms a. The mechanism involves carbocation intermediates b. The mechanism has two steps C. The reaction rate...
Organic chemistry. Can you please provide answer to this question. 1. There are various alkene constitutional...
Organic chemistry. Can you please provide answer to this
question.
1. There are various alkene constitutional isomers of the molecular formula C6H8 (two degrees of unsaturation). A few of those isomers (compounds A-F) were reacted under vigorous oxidation (with H3O+ and KMnO4) to yield specific products. Please provide the correct structure of the reactants and products in the corresponding boxes that fit the appropriate description. Draw dashes and wedges, where necessary, to show stereogenic centers. Note: you can assume that...
Predicting Products: Draw the structure of the one major organic product of each reaction in the...
Predicting Products: Draw the structure of the one major organic product of each reaction in the boxes provided. Be aware that the products all have the molecular formula C6H100, but oth products are constitutional isomers of one another. Stereochemistry should be shown if applicable. HO. Nah, DMSO Br HO, Nah, DMSO Br An efficient way to prepare asymmetrical ethers was developed by a British scientist, Alexander Williamson. Show what reagents you would use to prepare the following compound via a...
4. Redraw the following reactions with mechanistic details (i.e. show me the mechanism). The products are...
4. Redraw the following reactions with mechanistic details (i.e. show me the mechanism). The products are provided, and you do not deviate from them. Remember to use the curved arrows to show the movement of electrons and do not forget to indicate the charges. Be sure to clearly indicate any specific orientation needed in a reaction step, when it is necessary for the reaction. (5 points) DX mode on Y a D. X -
help Thank you 4. (10 pts) Draw all possible products for the following reaction including stereoisomers....
help Thank you
4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
1. Draw all constitutional isomers formed in the elimination reaction and predict the major product using the Zaitsev rule. A . KOCICH ! KOC(CH) 2. Draw all possible elimination reaction product(s) for the following alkyl halide. 4. Classify the following alkenes as mono, di-, tri, or tetra- substituted alkenes. Then, circle the most stable one. thayo by my 5. Which of the following alkenes is more stable?
QUESTION 4 What is the relationship between the following molecules? Br Br Br Identical Constitutional Isomers Diastereomers Enantiomers No relationship QUESTION 5 What is the relationship between the following molecules?
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
write the structures for all the alkene products that could
resonably be formed from each of the following compounds under yhe
indicated reaction.
4. Write the structures for all the alkene products (regio and stereo isomers) that could reasonably be formed from each of the following compounds under the indicated reaction conditions. Where more than one alkene is produced, specify the one that is the major product. (5) a. 3-Methyl-3-pentanol (sulfuric acid, 80°C) b. 2,3-Dimethyl-2-butanol (phosphoric acid, 120°C)
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label the mechanism as E2 or E1. a. 2-bromo butane reacts with methoxide b. 1-chloro-1-ethyl 2 methyl cyclopentane reacts with water 2. For which reaction mechanism are each of the following statements true? Mechanism S1, S2, E1 or E2. A statement may be true for one or more mechanisms a. The mechanism involves carbocation intermediates b. The mechanism has two steps C. The reaction rate...
Organic chemistry. Can you please provide answer to this
question.
1. There are various alkene constitutional isomers of the molecular formula C6H8 (two degrees of unsaturation). A few of those isomers (compounds A-F) were reacted under vigorous oxidation (with H3O+ and KMnO4) to yield specific products. Please provide the correct structure of the reactants and products in the corresponding boxes that fit the appropriate description. Draw dashes and wedges, where necessary, to show stereogenic centers. Note: you can assume that...
Predicting Products: Draw the structure of the one major organic product of each reaction in the boxes provided. Be aware that the products all have the molecular formula C6H100, but oth products are constitutional isomers of one another. Stereochemistry should be shown if applicable. HO. Nah, DMSO Br HO, Nah, DMSO Br An efficient way to prepare asymmetrical ethers was developed by a British scientist, Alexander Williamson. Show what reagents you would use to prepare the following compound via a...
4. Redraw the following reactions with mechanistic details (i.e. show me the mechanism). The products are provided, and you do not deviate from them. Remember to use the curved arrows to show the movement of electrons and do not forget to indicate the charges. Be sure to clearly indicate any specific orientation needed in a reaction step, when it is necessary for the reaction. (5 points) DX mode on Y a D. X -
help Thank you
4. (10 pts) Draw all possible products for the following reaction including stereoisomers. Note that the addition occurs through a "syn" mechanism. Is the product solution optically active (yes or no)? 1. BAHATHF 2. NaOH, HO (8 pts) Provide a complete mechanism for the reaction below and include lone-pairs of electrons and formal charges. Show all products formed including stereoisomers. Is the product solution optically active (yes or no)? Bras 11. (8 pts) Draw all four regiochemical...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
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