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.
The concept used to solve this problem is by using the given reagents, possible products will be formed in each step and then label it exactly in the given boxes in order to form the exact product.
Here, the starting reactant is alkene and the products are given different.
Bromine molecule is used for bromination of alkene. Trans addition takes place.
Addition of HBr to the double bond forms an alkyl bromide.
Sulfuric acid is used as a dehydrating agent.
Sodium methoxide is a strong base.
mCPBA is used for the epoxidation of alkene.
Hydration of alkene in the presence of sulfuric acid forms an alcohol.
Dehydrogenation of alkene in the presence of palladium catalyst gives alkane.
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
The reaction is as follows:
Ans:The appropriate reagents that are used for the given reactions are as follows:
Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated...
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.
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. Map Sapling Learning macmilan learning Fill in the appropriate reaets to achieve the synthetic transformation shown below. Note: If one or more reagents are incorrectly placed, a single re X appear on the top left 2. 3. 4. 5. Mg, ether NaH Br(CH2)2CH3 CH3(CH2ho NaOH CH3(CH2MgBr acetone H30*
Given the following chair conformation in the labeled box, place each label to identify the relationship of each structure to the boxed chair conformation. If one or more labels is incorrectly placed, a single red X will appear on the top left. Each label will only be used once.
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...
Drag and drop the labels onto the figure to identify the events associated with the cardiac cycle. Use each label once. Drag and drop the labels onto the figure to identify the events associated with the cardiac cycle. Use each label once. View Available Hint(s) Reset Help P wave I wave QRS wave Left atrial pressure diastolic Veitin dhe systolic pressure ventricular pressure Submit
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
Identify the oxidizing agent and the reducing agent for each reaction: Drag the appropriate labels to their respective targets.
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.
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.
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+