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1. For each of the following provide the structure of the final product(s) expected and state...
Please answer all parts for a good rating! Predict the product(s) for each of the following...
Please answer all parts for a good rating!
Predict the product(s) for each of the following reactions. Pay attention to stereochemistry. In each case, a reaction occurs, even if it is simply an acid-base reaction А) HO но H+ NaOEt Он C) pH 4~5 NH2 BL 2) Predict the organic product(s) at each step in the following reaction scheme. Also provide the complete arrow-pushing mechanism for the full process. You may use -Ph as an abbreviation for a benzene ring...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect this reaction to go easily (fast)? Explain your answers related to the mechanism and the rate of the reaction. CH,OH Q3-Circle only basic nitrogen atoms in the following structures. Q4 - Give the IUPAC name for the following molecule. o OH NO2 Q5 - Draw the structures of the following compounds. 2,6-dibromo-4-chloroanisole m-nitroacetophenone
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...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.)...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
Analyze the attached product NMR spectrum. Justify the structure of your final product and deduce the...
Analyze the attached product NMR spectrum. Justify the
structure of your final product and deduce the identity of your
unknown starting material.
Provide a reaction mechanism using the starting material that
you deduced in Qu. 1.
Experimental Procedure In this experiment. Vou will perform a double reductive amination reac an unknown aldehyde to form the corresponding amine product determine the identity of the unknown starting material. reaction between ethylenediamine and oduct. Analyze the lab data obtained to HẠN NHA RE...
1) Please provide the reaction pathway for the following (4pts each) Start a) Benzene End phenol...
1) Please provide the reaction pathway for the following (4pts each) Start a) Benzene End phenol Start End b) Benzene ortho cyanol phenol 2) Please provide the products and the type of reaction (SNI, SN2 El or E2) when given the reaction conditions- please use the temperatures stated (3pts each) a) CHs њо 22° C a) CHj K OC(CH3)s 3) Please Provide the Reactant and the conditions when given the product and mechanism type (3pts) CH3 (3° RX good L...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Please answer all parts for a good rating!
Predict the product(s) for each of the following reactions. Pay attention to stereochemistry. In each case, a reaction occurs, even if it is simply an acid-base reaction А) HO но H+ NaOEt Он C) pH 4~5 NH2 BL 2) Predict the organic product(s) at each step in the following reaction scheme. Also provide the complete arrow-pushing mechanism for the full process. You may use -Ph as an abbreviation for a benzene ring...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect this reaction to go easily (fast)? Explain your answers related to the mechanism and the rate of the reaction. CH,OH Q3-Circle only basic nitrogen atoms in the following structures. Q4 - Give the IUPAC name for the following molecule. o OH NO2 Q5 - Draw the structures of the following compounds. 2,6-dibromo-4-chloroanisole m-nitroacetophenone
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...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
Analyze the attached product NMR spectrum. Justify the
structure of your final product and deduce the identity of your
unknown starting material.
Provide a reaction mechanism using the starting material that
you deduced in Qu. 1.
Experimental Procedure In this experiment. Vou will perform a double reductive amination reac an unknown aldehyde to form the corresponding amine product determine the identity of the unknown starting material. reaction between ethylenediamine and oduct. Analyze the lab data obtained to HẠN NHA RE...
1) Please provide the reaction pathway for the following (4pts each) Start a) Benzene End phenol Start End b) Benzene ortho cyanol phenol 2) Please provide the products and the type of reaction (SNI, SN2 El or E2) when given the reaction conditions- please use the temperatures stated (3pts each) a) CHs њо 22° C a) CHj K OC(CH3)s 3) Please Provide the Reactant and the conditions when given the product and mechanism type (3pts) CH3 (3° RX good L...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
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