Draw all the products of the acid-base reaction between the species shown below. Use only one equivalent of OH- in this reaction. Interactive 3D display mode ΟΗΤ HO ΌΗ
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- app.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F6Curved arrows are used to illustrate the flow of electrons. In this reaction, a pi bond acts as a Bronsted base. Using the provided starting structures, draw the curved electron- pushing arrows for the acid-base reaction. Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of the reaction. + Include all lone pairs in the structures. Ignore inorganic byproducts and counterions. I I HH :CI. co THE I Select to Edit ArrowsGive a complete arrow-pushing mechanism for the following reactions. Show all important resonance structures of the intermediates and show exactly where each proton comes from and goes to. Indicate the Lewis acid and Lewis base (LA or LB) and whether they are also Bronsted acids and bases (BA or BB) for each intermolecular reaction. To preview image Click Here EtOH HCI (cat.) 0 LOEt OEt + H₂O
- 3) Use the reaction shown below and the associated reaction energy diagram to answer the following questions. E A Но- + Br HO. Br- reaction coordinate a) In the space above, use curved arrows to show the mechanism of the reaction. b) Classify the reaction as either addition, elimination or substitution. c) In this reaction is hydroxide (HO-) acting as a nucleophile or as a base? c) Based on the reaction energy diagram, is the reaction endergonic or exergonic? d) Based on the reaction energy diagram, and assuming the reaction is reversible, would the equilibrium lie to the left or to the right? e) Which position on the reaction energy diagram (A, B or C) corresponds to the transition state?7. (Chapters 6 and 8) Within the following set, which is more stable, and why? CH3 CH3 H3C- -C=CH- CH2 H2C=Ć- -CH CH3 8. (Chapter 12) What type of instability will an intermediate need to address following the reaction of a nucleophile/base that has a negative charge with a pi bond that has uneven electron distribution between atoms with different electronegativities (C=O)? 9. (Chapter 9) Circle the carbon that will be unstable in the intermediate of the following reaction. Then, state the reason for your choice, and also indicate what type of instability it will be. H,C-CH,- C ECH with NaNH2 10. (Chapters 12 and 13) What are three sources used to provide electrons to an electron-deficient carbon with a leaving group? 1. 2. 3.Answer all three parts plz. You are starting with three aryl bromides. They undergo a typical grignard reaction with magnesium metal and anhydrous ether (diethyl ether). Dry ice is then added to it and it is then cooled. Draw and label the names of the aryl carboxylic acids that will form for each. Part a) bromobenzene Part b) para-bromoanisole Part c) meta-bromoanisole
- helpCurved arrows are used to illustrate the flow of electrons. In this reaction, a pi bond acts as a Bronsted base. Using the provided starting structures, draw the curved electron-pushing arrows for the acid-base reaction. Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of the reaction. Include all lone pairs in the structures. Ignore inorganic byproducts and counterions. H. | H H :CIⒸ Select to Add ArrowsDraw the structure of the product of the reaction between the compound shown below and H,SO. CH3COCH2CH3 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If the reaction involves proton transfer, draw the products in separate sketchers. • If the reaction is a Lewis acid-base reaction, draw the product in one sketcher only. CP opy aste 翻 券 網
