Fill in the appropriate reagents to achieve the synthetic transformation shown below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left.
Homework Answers
Reagents are the substances used to transform one substance to another. The organic reactions involve the conversion of one or more functional groups to other useful functional groups using wide range of reagents.
The reagents play a vital role in a reaction to undergo a transformation. Each reagent plays a different role in the chemical reaction.
: It makes the Grignard reagent.
: This makes organometallic reagent to alcohol.
Sodium hydride: Strong base and useful to remove protons.
Alkyl halide: Useful to synthesis alcohol to ether.
Hence, the ether product formed in the reaction as follows:
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Fill in the appropriate reagents to achieve the synthetic transformation shown below. Note: If one or more reagents are...
Shown below is the synthesis of N,N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents to...
Shown below is the synthesis of N,N-dimethyl-2-methylhexanamide
from diethyl malonate. Fill in the best reagents to achieve this
synthetic transformation. Note: If one or more reagents are
incorrectly placed, a single red X will appear on the top left.
Select the missing reagents needed to convert each molecule into the next one pictured in the...
Select the missing reagents needed to convert each molecule into
the next one pictured in the synthetic scheme below. Note: If one
or more reagents are incorrectly placed, a single red X will appear
on the top left.
Select the missing reagents needed to convert each molecule into the next one pictured in the synthetic scheme below. Note: Ifone or more reagents are incorrectly placed, a single red X will appear on the top left. 1. acetone Brz. CH3CH2OH H30...
Label the reaction with the reagents necessary to facilitate the transformation below. Note that if one...
Label the reaction with the reagents necessary to facilitate the transformation below. Note that if one or more reagents are incorrectly placed, a single red X will appear on the top left.
Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated...
Drag the labels to identify the appropriate reagents for each
reaction below. Each label is associated with the arrow adjacent to
it. The direction of the arrow is important! Note: If one or more
reagents are incorrectly placed, a single red X will appear on the
top left.
Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated with the arrow adjacent to it. The direction of the arrow is important! Note: If one...
In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route...
In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. CH3CHO, 2H2O CH2CH2CH2CHO, 2H2O CH3(CH2)2MgBr, H2O CH3MgBr, H2O CH3(CH2)2OH Mg CH3Br PCC HOCH2CH2OH, H+ H3O+
18 Classify the following solvents as either protic or aprotic solvents. Note: If one or more solvents are incorrect...
18
Classify the following solvents as either protic or aprotic solvents. Note: If one or more solvents are incorrectly placed, a single red X will appear on the top left. Protic Aprotic DMF DMso acetonitrile acetone H20 cH3CH20H CH3OH acetic acid
Label each carbon atom with its optimum C-C-C bond angle. Note: If one or more bond...
Label each carbon atom with its optimum C-C-C bond angle. Note: If one or more bond angles are incorrectly placed, a single red X will appear on the top left CH3 H3 degrees CH2 ← 180 degrees 109.5 degr CH CH3
Starting with cyclohexene, propose a reasonable synthesis of the cyclohexene derivative below. If one or more...
Starting with cyclohexene, propose a reasonable synthesis of the cyclohexene derivative below. If one or more reagents are incorrectly placed, a single red X will appear on the top left.
In each reaction box, place the best reagent and conditions from the list below. Note: If...
In each reaction box, place the best reagent and conditions from the list below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. он 2. 3. он он
Shown below is the synthesis of N, N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents...
Shown below is the synthesis of N, N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents to achieve this synthetic transformation.
Shown below is the synthesis of N,N-dimethyl-2-methylhexanamide
from diethyl malonate. Fill in the best reagents to achieve this
synthetic transformation. Note: If one or more reagents are
incorrectly placed, a single red X will appear on the top left.
Select the missing reagents needed to convert each molecule into
the next one pictured in the synthetic scheme below. Note: If one
or more reagents are incorrectly placed, a single red X will appear
on the top left.
Select the missing reagents needed to convert each molecule into the next one pictured in the synthetic scheme below. Note: Ifone or more reagents are incorrectly placed, a single red X will appear on the top left. 1. acetone Brz. CH3CH2OH H30...
Label the reaction with the reagents necessary to facilitate the transformation below. Note that if one or more reagents are incorrectly placed, a single red X will appear on the top left.
Drag the labels to identify the appropriate reagents for each
reaction below. Each label is associated with the arrow adjacent to
it. The direction of the arrow is important! Note: If one or more
reagents are incorrectly placed, a single red X will appear on the
top left.
Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated with the arrow adjacent to it. The direction of the arrow is important! Note: If one...
In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. CH3CHO, 2H2O CH2CH2CH2CHO, 2H2O CH3(CH2)2MgBr, H2O CH3MgBr, H2O CH3(CH2)2OH Mg CH3Br PCC HOCH2CH2OH, H+ H3O+
18
Classify the following solvents as either protic or aprotic solvents. Note: If one or more solvents are incorrectly placed, a single red X will appear on the top left. Protic Aprotic DMF DMso acetonitrile acetone H20 cH3CH20H CH3OH acetic acid
Label each carbon atom with its optimum C-C-C bond angle. Note: If one or more bond angles are incorrectly placed, a single red X will appear on the top left CH3 H3 degrees CH2 ← 180 degrees 109.5 degr CH CH3
Starting with cyclohexene, propose a reasonable synthesis of the cyclohexene derivative below. If one or more reagents are incorrectly placed, a single red X will appear on the top left.
In each reaction box, place the best reagent and conditions from the list below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. он 2. 3. он он
Shown below is the synthesis of N, N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents to achieve this synthetic transformation.
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