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N gCIL Drawing Resonance Contributors of Substituted Benzenes Identify the functional groups attached to the benzene...
Question 3 1s 3 ORTHO Today we learned about adding a second group to a mono-substituted...
Question 3
1s 3 ORTHO Today we learned about adding a second group to a mono-substituted benzene ring. Any group on a benzene will affect the rate of the reaction (activated or deactivated relative to benzene) and the regioselectivity Where does the electrophile add? Ortho? Meta? Para? Some combination thereof? We found that EDGs (electron-donating groups) direct the electrophile to the ortho and para positions while EWGs (electron-withdrawing groups) direct the electrophile to the meta position. Now, it is time...
Assume the functional groups below are attached to a benzene ring. Circle the functional groups that...
Assume the functional groups below are attached to a benzene ring. Circle the functional groups that are activating. Put a triangle around those that are deactivating. Predict the directing effect of each group (either o,p or m). Do you see any trends? {-Br 4-CF3 OCH3 {NH2 & NH3 NO2 &-coh 10
Synthesis of disubstituted benzenes involves two steps, each introducing one of the functional groups For the...
Synthesis of disubstituted benzenes involves two steps, each introducing one of the functional groups For the synthesis of p-chlorosulfonic acid, select the reagent for each step and draw the structure of the monosubstituted intermediate compound. Put the intermediate substituent in the same place that it is oberved in the product (i.e. either the top or the bottom of the benzene ring). Intermediate Step 1 Step 2 O C2, peroxide O Ch. FeCl3 O SOs, H2S04 O Cl2. peroxide O Cl2....
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each item to the appropriate bin. ► View Available Hint(s) Reset Help OH CH3CH2-N CH3CH2 CH3CH2C-NCH3 Н CH,C- N 1 CH CH CH CH COCH CH3CCH2CH3 CH,CH.CH Amine Amide Neither amine nor amide Part B Classify each molecule as an aldehyde, ketone, or neither. Drag each item to the appropriate bin. View Available Hint(s) Reset Help propanoic acid) (3 regtanone (C1,C1,0 mostry hoxancato nocara (C1;OCIĄT3...
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...
Question 3
1s 3 ORTHO Today we learned about adding a second group to a mono-substituted benzene ring. Any group on a benzene will affect the rate of the reaction (activated or deactivated relative to benzene) and the regioselectivity Where does the electrophile add? Ortho? Meta? Para? Some combination thereof? We found that EDGs (electron-donating groups) direct the electrophile to the ortho and para positions while EWGs (electron-withdrawing groups) direct the electrophile to the meta position. Now, it is time...
Assume the functional groups below are attached to a benzene ring. Circle the functional groups that are activating. Put a triangle around those that are deactivating. Predict the directing effect of each group (either o,p or m). Do you see any trends? {-Br 4-CF3 OCH3 {NH2 & NH3 NO2 &-coh 10
Synthesis of disubstituted benzenes involves two steps, each introducing one of the functional groups For the synthesis of p-chlorosulfonic acid, select the reagent for each step and draw the structure of the monosubstituted intermediate compound. Put the intermediate substituent in the same place that it is oberved in the product (i.e. either the top or the bottom of the benzene ring). Intermediate Step 1 Step 2 O C2, peroxide O Ch. FeCl3 O SOs, H2S04 O Cl2. peroxide O Cl2....
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Organic Functional Groups Part A Classify each molecule as an amine, amide, or neither. Drag each item to the appropriate bin. ► View Available Hint(s) Reset Help OH CH3CH2-N CH3CH2 CH3CH2C-NCH3 Н CH,C- N 1 CH CH CH CH COCH CH3CCH2CH3 CH,CH.CH Amine Amide Neither amine nor amide Part B Classify each molecule as an aldehyde, ketone, or neither. Drag each item to the appropriate bin. View Available Hint(s) Reset Help propanoic acid) (3 regtanone (C1,C1,0 mostry hoxancato nocara (C1;OCIĄT3...
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...
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