Homework Answers
This reaction takes place via SN1 reaction.
Here the formed carbocation under goes resonance to form more stable allylic carbocation. Here, Two intermediates are formed so two products are formed in this reaction.
This is SN1 reaction so the rate of reaction only depends on concentration of alkyl halide.
Because of this reason addition of acetate ion doesn't effect the rate of reaction.
The mechanism of the reaction as follows:
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4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating...
help please! for 6 and 7. 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one...
help please! for 6 and 7.
6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH CH,O to give an elimination product. Provide the structure of this compound and briefly explain why it does not react (5 points). When 4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are formed, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction...
please help with organic chemistry! mechanisms? 5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following...
please help with organic chemistry! mechanisms?
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...
give the name of the major product formed shen HCl reacts with 2-pentene Give the name...
give the name of the major product formed shen HCl reacts with
2-pentene
Give the name of the major product formed when HCl reacts with 2-pentene. O 3-chloropentane O 2,3-dichloropentane O 24hloropentane O There are no major or minor products. There is a 50/50 mixture of both O The reaction doesn't occur.
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major)....
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of alcohol and oxygen to form anoxonium ion.Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products ofthis reaction.The 3.) is correct that is the minor product I came up with but I cant get the answer correct for 1.) major product? and 2.) minor product
5. Upon reaction of 3-methyl-4-phenyl-2-heptanol with concentrated aqueous hydrochloric acid, the major product 4-chloro-3-methyl-4-phenylheptane was found....
5. Upon reaction of 3-methyl-4-phenyl-2-heptanol with concentrated aqueous hydrochloric acid, the major product 4-chloro-3-methyl-4-phenylheptane was found. Show the mechanism for this reaction.
Dropdown Menus: 1. methyl, primary (unhindered), primary (hindered), secondary, tertiary 2. poor, weakly basic, strongly basic...
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
1. Write equations for the reactions that occur in the following. (a) 2-methylbutanol and acetic acid...
1. Write equations for the reactions that occur in the following. (a) 2-methylbutanol and acetic acid (ethanoic acid) are heated together in the presence of a small quantity of sulphuric acid. (b) Butanoic acid is added to a solution of thionyl chloride (SOCl2) and the mixture heated. After the reaction has occurred an excess of diethyl amine is added. 2. (a) How would you separate a mixture of benzoic acid and dibutyl amine, using a 1M HCl solution, a 1M...
the weight if the initial product was 3.4 grams of methyl benzoate. Who |o yald foR 3.91SSg st prodoc...
the
weight if the initial product was 3.4 grams of methyl
benzoate.
Who |o yald foR 3.91SSg st prodoct nd product 2.14143 EXPERIMENTAL PROCEDURE SAFETY WEAR nitrile gloves for this experiment. The nitrating moture of sulfuric acidnitric acid (1:1) is a very strong acid system. Do not allow it to come in contact with your skin or clothing. It will cause acid burns if it comes in contact with your skin (and holes an your clothes). Wash any affected area...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
help please! for 6 and 7.
6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH CH,O to give an elimination product. Provide the structure of this compound and briefly explain why it does not react (5 points). When 4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are formed, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction...
please help with organic chemistry! mechanisms?
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...
give the name of the major product formed shen HCl reacts with
2-pentene
Give the name of the major product formed when HCl reacts with 2-pentene. O 3-chloropentane O 2,3-dichloropentane O 24hloropentane O There are no major or minor products. There is a 50/50 mixture of both O The reaction doesn't occur.
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of alcohol and oxygen to form anoxonium ion.Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products ofthis reaction.The 3.) is correct that is the minor product I came up with but I cant get the answer correct for 1.) major product? and 2.) minor product
5. Upon reaction of 3-methyl-4-phenyl-2-heptanol with concentrated aqueous hydrochloric acid, the major product 4-chloro-3-methyl-4-phenylheptane was found. Show the mechanism for this reaction.
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
1. Write equations for the reactions that occur in the following. (a) 2-methylbutanol and acetic acid (ethanoic acid) are heated together in the presence of a small quantity of sulphuric acid. (b) Butanoic acid is added to a solution of thionyl chloride (SOCl2) and the mixture heated. After the reaction has occurred an excess of diethyl amine is added. 2. (a) How would you separate a mixture of benzoic acid and dibutyl amine, using a 1M HCl solution, a 1M...
the
weight if the initial product was 3.4 grams of methyl
benzoate.
Who |o yald foR 3.91SSg st prodoct nd product 2.14143 EXPERIMENTAL PROCEDURE SAFETY WEAR nitrile gloves for this experiment. The nitrating moture of sulfuric acidnitric acid (1:1) is a very strong acid system. Do not allow it to come in contact with your skin or clothing. It will cause acid burns if it comes in contact with your skin (and holes an your clothes). Wash any affected area...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
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