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

ment - Basic Chemistry CHE 210... gnment Score: stion 1 of 25 > O Macmillan Learning $ 4 R reaction: 89.3% F4 A carboxylic acid reacts with water to form a carboxylate ion and H₂O+. Complete the reaction. IUPAC name: VI SPECIAL e Write the IUPAC name of the carboxylate ion formed in the reaction. C6H₂COOH + H₂O= 5 5 IV M % T # B GA carboxylic acid reacts with water to for... 9 F5 achieve.macmillanlearning.com GREEK ALPHABET 22 1 6 U ४ X Y X2 F6 MacBook Air x² 7 + 3 F7 U * 00 8 ∞ G A carboxylic acid reacts with water to for... Resources ➡ Give Up? 1 C DII F8 E ( 9 ▷▷ F9 0 0 B F10 Hint P GA carboxylic acid reacts with F11 1 Check Answer Attempt 3 F12

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Explain the differences in pKa (vs. benzoic acid) of these substituted benzoic acids based on fundamental chemical principles (not just what pKa means).

The blcyclic ketone shown below is first treaterd with a base, then ethyliodide is added to form the substituted ketone. Which base/conditions are sultable? 1) Base 2) O 1. Lithium diisopropylamide in THF at -78 "C. O 2. NaBH4 in methanol at room temperature. O 3. Sodium methoxide in methanol at room temperature. O 4. DBU in THF at 25 "C.

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

Carboxylic Acid Derivatives Resolve the reactions.

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

1. Propose a synthetic route from the starting material to the product. Show each individual reaction step and all intermediate products. Assume acidic workups occur if needed. Starting Material Product 4. b. Br Starting Material محمد مجار Product Joi OH >= ОН c. Hint: Number the carbons in your starting material and your product. ОН Starting Material Product OH OH