Homework Answers
when alkylhalides reacts with alkoxide I.e strong base it undergoes elimination and forms the alkene product and it undergoes hydroboration oxidation reaction it produces the primary alcohol as shown below
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2. (5 pts.) Show hoe the following transformation could occur. The reaction may require more than...
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may...
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may be needed. Show all reagents and synthetic intermediates.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions th...
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions...
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit. 2. For the compound shown in the box to the right, provide an IUPAC compliant name, including all stereochemical details.
Each of the following syntheses may require more than one step. Provide the reagents and intermediates...
Each of the following syntheses may require more than one step.
Provide the reagents and intermediates for each step from the
starting reagent to the final product.
H H and prepare CH3CH-CH2 (a) Start with CH3 CH3 and prepare (b) Start with OC(CH3)3 and prepare and any 2 carbon fragment (c) Start with CH3CH CH2 СH, and prepare (d) Start with
Please help 2. (pts) The following transformations require 5-6 steps. Show how to accomplish the transformations...
Please help
2. (pts) The following transformations require 5-6 steps. Show how to accomplish the transformations below using benzene as the starting material and any other monounctional organic reagents and inorganic reagents. To maximize your chances for partial credit show the products obtained after each step. Mechanisms should NOT be included. Your best 1 of 2 will be graded. отьору OH
Design a Synthesis: Show both the retrosynthetic analysis, as well as the forward synthetic scheme. The overall transformation may require more than one step. Design a Synthesis: Show both t...
Design a Synthesis: Show both the retrosynthetic analysis, as well as the forward synthetic scheme. The overall transformation may require more than one step.
Design a Synthesis: Show both the retrosynthetic analysis, as well as the forward synthetic scheme. The overall transformation may require more than one step.
31) Provide the reagents necessary to complete the following transformation. More than one step is needed....
31) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. CH он 32) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. Br он enantiomer HO tto prss 33) Provide the reagents necessary to convert 3-methyl-2-butanol into 2-methyl-2-butanol. More than step is needed. Show the structures of any intermediate products. Page 7 of 8
Propose a synthesis to carry out the following transformation, using any reagents necessary. Note: This may...
Propose a synthesis to carry out the following transformation, using any reagents necessary. Note: This may require more than one step! > al? OY
2) Show how you would carry out the following transformation, using any reagents necessary (requires more...
2) Show how you would carry out the following transformation, using any reagents necessary (requires more than one step). 2 CN
Provide a mechanism for the following reaction. Please show all intermediates and use arrows to show...
Provide a mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons. Propose a synthesis for the following compound. You may use any reagents needed. Complete the synthesis in 4 steps or less (more than one step is needed).
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may be needed. Show all reagents and synthetic intermediates.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit. 2. For the compound shown in the box to the right, provide an IUPAC compliant name, including all stereochemical details.
Each of the following syntheses may require more than one step.
Provide the reagents and intermediates for each step from the
starting reagent to the final product.
H H and prepare CH3CH-CH2 (a) Start with CH3 CH3 and prepare (b) Start with OC(CH3)3 and prepare and any 2 carbon fragment (c) Start with CH3CH CH2 СH, and prepare (d) Start with
Please help
2. (pts) The following transformations require 5-6 steps. Show how to accomplish the transformations below using benzene as the starting material and any other monounctional organic reagents and inorganic reagents. To maximize your chances for partial credit show the products obtained after each step. Mechanisms should NOT be included. Your best 1 of 2 will be graded. отьору OH
Design a Synthesis: Show both the retrosynthetic analysis, as well as the forward synthetic scheme. The overall transformation may require more than one step.
Design a Synthesis: Show both the retrosynthetic analysis, as well as the forward synthetic scheme. The overall transformation may require more than one step.
31) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. CH он 32) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. Br он enantiomer HO tto prss 33) Provide the reagents necessary to convert 3-methyl-2-butanol into 2-methyl-2-butanol. More than step is needed. Show the structures of any intermediate products. Page 7 of 8
Propose a synthesis to carry out the following transformation, using any reagents necessary. Note: This may require more than one step! > al? OY
2) Show how you would carry out the following transformation, using any reagents necessary (requires more than one step). 2 CN
Provide a mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons. Propose a synthesis for the following compound. You may use any reagents needed. Complete the synthesis in 4 steps or less (more than one step is needed).
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