What is the predicted final product of the reaction sequence shown? diethyl malonate 1. sodium ethoxide 1. sodium ethoxide H3O+ A 2. 1-bromopentane 2. bromomethane O 2-methylheptanoic acid 3-methylhexanoic acid O 3-methylpentanoic acid O 2-methylpentanoic acid O ethyl 2-methylheptanoate

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Question 24 please and thank you! It's an exam study guide so it's not for a grade.

following reactions. a. HO b. HO OH OH NH₂ NH₂ H₂SO4 H₂O + 1. LIAIH4 2. H* workup Imine Formation trace acid

9. Which of the reagents listed below will convert benzene to methyl benzoate? Methyl benzoate 1. CICH,CH3 2. KMnO4 1. Br2, FeBr3 2. СО, МеОН 1. Brz, FeBr3 2. Mg CICOOCH3, AICI3 E. None of these 3. МеОН, Н* A C D

A series of extractions is performed to separate cyclohexylamine 1, 4-methylpentanoic acid 2, and trans-decalin 3. Where will the cyclohexylamine 1 and 4-methylpentanoic acid 2 be found? (*` H20 A NH2 H20 1. aq. NaOH 2. ether В ether HO 1. aq. HCI H20 2 2. ether H20 1. aq. HCI 2. ether D ether 1. aq. NaOH ether 2. ether + E ether A. 1= B, 2 = A B. 1= B, 2 = C C. 1= B, 2 = D D. 1= E, 2 = A E. 1= E, 2 = B F. 1= E, 2 = D Enter Your Answer: O A Ов Ос ОЕ ОF

Draw structural formulas for organic products A and B in the window below. H₂O Mg ether ● ● ● H3CC=CH₂ Br *8 Draw only products having the organic portion of the original alkyl halide. Draw carbon-lithium bonds using the single bond tool. If a structure has a copper-lithium bond, do not draw the lithium. Separate products from different steps using the → sign from the drop-down menu. ? A Ⓡ ChemDoodle B Sn [F

20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat C

The bicyclic ketone shown below is first treaterd with a base, then ethyliodide is added to form the substituted ketone. Which base/conditions are suitable? 1) Base 2) O 1. Lithium disopropylamide in THF at -78 *C. O 2. NABH4 in methanol at room temperature. 3. Sodium methoxide in methanol at room temperature. O 4. DBU in THF at 25 "C.