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Please help. It's asking for two mechanisms, one from the
alkyl halide to the carboxylic acid...
"Carboxylic acids can be made by the hydrolysis of nitriles, which in turn can be made from an alkyl halide. Draw the...
"Carboxylic acids can be made by the hydrolysis of nitriles,
which in turn can be made from an alkyl halide. Draw the structures
of a starting alkyl bromide and the intermediate nitrile that would
be used in the synthesis of 3-methylbutanoic acid (also known as
isovaleric acid). Do not show free ions."
I answered the first part right but it is saying that the
second part is incorrect. On my carbon that is triple bonded to the
nitrogen has a...
Carboxylic acids can be made by the hydrolysis of nitriles, which in turn can be made from an alkyl halide. Draw the st...
Carboxylic acids can be made by the hydrolysis of nitriles, which
in turn can be made from an alkyl halide. Draw the structures of a
starting alkyl bromide and the intermediate nitrile that would be
used in the synthesis of 3-methylbutanoic acid (isovaleric acid) Do
not show free ions.
alkyl bromide nitrile isovaleric
acid
Carboxylic acids can be made by the hydrolysis of nitriles, which in turn can be made from an alkyl halide. Draw t...
Carboxylic acids can be made by the hydrolysis of nitriles, which in turn can be made from an alkyl halide. Draw the structures of a starting alkyl bromide and the intermediate nitrile that would be used in the synthesis of 3-methylbutanoic acid (also known as isovaleric acid). Do not show free ions.
Please help with this mechanism Draw the mechanism for the reaction of an alkyl halide with...
Please help with this mechanism
Draw the mechanism for the reaction of an alkyl halide with sodium azide, followed by reduction. Follow the directions on each step. Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium Complete the product structure by adding any missing atoms, bonds, charges, and nonbonding electrons. Omit curved arrows. Predict the organic product of the LAH reduction and hydrolysis steps; include nonbonding electrons. Do not include any inorganic products.
pleas help 5,6,7,8,9,10 III IV 5. The product of free-radical halogenation reactions is an alkyl halide....
pleas help 5,6,7,8,9,10
III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
i need help with these but alkene is the major product formed from each alkyl halide...
i need help with these
but alkene is the major product formed from each alkyl halide in an El reaction? CH Br CHE Considering the requirement of an anti-periplanar geometry, what E2 product(s) is/are formed from each starting material? Note: Deuterium (Atomic Symbol: D) is one of the two stable isotopes of hydrogen."It nucleus contains one proton and one neutron, whereas the nucles of the more common isotope, protium, contains only one profon. The heavier version of hydrogen can undergo...
help me to answer question b please.. 6.51 Consider the conversion of alkyl halide A to...
help me to answer question b please..
6.51 Consider the conversion of alkyl halide A to ether B. -Bra O OCH3 + CH2OH + HB a. Classify the conversion of A to B as substitution, elimination, or addition. b. The reaction rate depends on the concentration of A only. Write the rate equation for the reaction, and explain why the reaction mechanism must involve more than one step.
Provide three examples (both structure and name for each case) for the following carboxylic acid and...
Provide three examples (both structure and name for each case) for the following carboxylic acid and its derivatives (a) Carboxylic acid (b) Acid halide (c) Acid anhydride (d) Ester (e) Thioester (0) Amide 1. 6x3-18 2. Write a preparation method for one compound from each category in question 1 . 6x2-12 The following two are the general reaction mechanisms for carbonyl group containing compounds. What is the difference between them? Write mechanism from a reaction describe in question 2. 3....
help please! Propose the best synthetic route to do the following transformation Draw dearly the different...
help please!
Propose the best synthetic route to do the following transformation Draw dearly the different intermediates indicating their stereochemistry if present. (More than one step it needed). Propose a complete and detailed mechanism for the products to the following reaction Propose a synthetic route to produce the following alkyl halides from the starting material given. And draw the complete mechanism for the synthesis. Devise a stepwise mechanism for the following reaction Draw the products of the following reaction, indicating...
The carboxylic acid shown below may be prepared easily from all but one of the substrates....
The carboxylic acid shown below may be prepared easily from all
but one of the substrates. Which compound would not provide easy
synthesis of the acid?
The carboxylic acid shown below may be prepared easily from all but one of the substrates. Which compound would not provide easy synthesis of the acid? OH сн. Br a. COH CN OH a. b. c. d.
"Carboxylic acids can be made by the hydrolysis of nitriles,
which in turn can be made from an alkyl halide. Draw the structures
of a starting alkyl bromide and the intermediate nitrile that would
be used in the synthesis of 3-methylbutanoic acid (also known as
isovaleric acid). Do not show free ions."
I answered the first part right but it is saying that the
second part is incorrect. On my carbon that is triple bonded to the
nitrogen has a...
Carboxylic acids can be made by the hydrolysis of nitriles, which
in turn can be made from an alkyl halide. Draw the structures of a
starting alkyl bromide and the intermediate nitrile that would be
used in the synthesis of 3-methylbutanoic acid (isovaleric acid) Do
not show free ions.
alkyl bromide nitrile isovaleric
acid
Carboxylic acids can be made by the hydrolysis of nitriles, which in turn can be made from an alkyl halide. Draw the structures of a starting alkyl bromide and the intermediate nitrile that would be used in the synthesis of 3-methylbutanoic acid (also known as isovaleric acid). Do not show free ions.
Please help with this mechanism
Draw the mechanism for the reaction of an alkyl halide with sodium azide, followed by reduction. Follow the directions on each step. Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium Complete the product structure by adding any missing atoms, bonds, charges, and nonbonding electrons. Omit curved arrows. Predict the organic product of the LAH reduction and hydrolysis steps; include nonbonding electrons. Do not include any inorganic products.
pleas help 5,6,7,8,9,10
III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
i need help with these
but alkene is the major product formed from each alkyl halide in an El reaction? CH Br CHE Considering the requirement of an anti-periplanar geometry, what E2 product(s) is/are formed from each starting material? Note: Deuterium (Atomic Symbol: D) is one of the two stable isotopes of hydrogen."It nucleus contains one proton and one neutron, whereas the nucles of the more common isotope, protium, contains only one profon. The heavier version of hydrogen can undergo...
help me to answer question b please..
6.51 Consider the conversion of alkyl halide A to ether B. -Bra O OCH3 + CH2OH + HB a. Classify the conversion of A to B as substitution, elimination, or addition. b. The reaction rate depends on the concentration of A only. Write the rate equation for the reaction, and explain why the reaction mechanism must involve more than one step.
Provide three examples (both structure and name for each case) for the following carboxylic acid and its derivatives (a) Carboxylic acid (b) Acid halide (c) Acid anhydride (d) Ester (e) Thioester (0) Amide 1. 6x3-18 2. Write a preparation method for one compound from each category in question 1 . 6x2-12 The following two are the general reaction mechanisms for carbonyl group containing compounds. What is the difference between them? Write mechanism from a reaction describe in question 2. 3....
help please!
Propose the best synthetic route to do the following transformation Draw dearly the different intermediates indicating their stereochemistry if present. (More than one step it needed). Propose a complete and detailed mechanism for the products to the following reaction Propose a synthetic route to produce the following alkyl halides from the starting material given. And draw the complete mechanism for the synthesis. Devise a stepwise mechanism for the following reaction Draw the products of the following reaction, indicating...
The carboxylic acid shown below may be prepared easily from all
but one of the substrates. Which compound would not provide easy
synthesis of the acid?
The carboxylic acid shown below may be prepared easily from all but one of the substrates. Which compound would not provide easy synthesis of the acid? OH сн. Br a. COH CN OH a. b. c. d.
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