Ethers Questions

Organic Chemistry

Ethers Solutions

Dilute, aqueous sulfuric acid is generally used to promote acid catalyzed hydration because: (A) these conditions have excess reactant and therefore drive the reaction towards products. (B) these conditions have excess product and therefore drive the reaction towards products. (C) these conditions remove product and therefore drive the reaction towards products. (D) these conditions remove reactant and therefore drive the reaction towards products.

Organic Chemistry

Ethers Solutions

Dilute, aqueous sulfuric acid is generally used to promote acid catalyzed hydration because: these conditions have excess reactant and therefore drive the reaction towards products. these conditions have excess product and therefore drive the reaction towards products. these conditions remove product and therefore drive the reaction towards products. these conditions remove reactant and therefore drive the reaction towards products.

Organic Chemistry

Ethers Solutions

Dilute, aqueous sulfuric acid is generally used to promote acid catalyzed hydration because: these conditions have excess reacta Dilute, aqueous sulfuric acid is generally used to promote acid catalyzed hydration because: Othese conditions have excess reactant and therefore drive the reaction towards products. Othese conditions have excess product and therefore drive the reaction towards products. O these conditions remove product and therefore drive the reaction towards products. these conditions remove reactant and therefore drive the reaction towards products. Q

Organic Chemistry

Ethers Solutions

O OR group HO A hemiacetal is a compound with both an alcohol-like -OH group and an ether-like- bonded to the same carbon atom. An acetal is a compound that has two ether-like -OR groups bonded to the same carbon atom. OH O Identify the structure that contains an acetal. HO HO CH HO

Organic Chemistry

Ethers Solutions

Part 2: Practice Problems: Follow steps 1-5 to illustrate the synthesis of the following alcohols: a) dipropyl ether Step 1: Draw Kekule structures of the reagents: Step 2: Mark reacting atoms, group, or bonds: Step 3: Indicate proton and hydroxide groups to be removed. Step 4: Write Kekule structure of the product.

Organic Chemistry

Ethers Solutions

Draw the missing organic structures or select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed. 0 1. NaOCH2CH3 li Select to Draw 2. (CH3)2CHCI (1 equiv) 1. NaOCH2CH3 2. CHBr 11 equiv) H30* Select to Draw Select to Draw heat

Organic Chemistry

Ethers Solutions

Question 3 1 pts Which of the following three compounds can be readily synthesized by a Williamson ether synthesis reaction? O A B C (a) A and C (b) B only (c) C only (d) B and C (e) all of A, B and C a b Oc Od Oe MacBook Pro C Search or type URL 7 $ % &

Organic Chemistry

Ethers Solutions

Using the reaction bank, devise a synthetic route (should use several reactions) to convert the starting material into the product. Remember, order is important. Reaction Bank: N A: SOCI ola OCH3 B: H2O, NaOH C: NH3 Step 1: Reaction A Step 2: Reaction B Step 3: Reaction C Step 1: Reaction C Step 2: Reaction A Step 1: Reaction C Step 2: Reaction B Step 3: Reaction A Step 1: Reaction B Step 2: Reaction A

Organic Chemistry

Ethers Solutions

ontents This is a graded discussion: 2 points possible Week 10: Chapter 18 Discussion: Esterification reactions Name a few sweet smelling esters Name a carboxylic acid and an alcohol which can produce the following esters: a) ethyl acetate b) methyl benzoate c) Isopropyl fomate 2 Search entries or author Unread 2 brations

Organic Chemistry

Ethers Solutions

Ethers can be prepared by reaction of an alkoxide or phenoxide ion with a primary alkyl halide. Draw the structure of the expected organic product of the reaction of lodoethane with the following alkoxide ion: H3C CH3 + Na • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Do not include counter-ions, e.g., Nat, I", in your answer. C opy P BE -0%

Organic Chemistry

Ethers Solutions

Review Topice Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is treated with aqueous NaOH. SH + NaOH CH . You do not have to consider stereochemistry . You do not have to explicitly draw Hatoms. . Include counter-ions, e.g., Na+, 1", in your submission, but draw them in their own separate sketcher. . If no reaction occurs, draw the organic starting material. CP 0000 ChemDoodle Submit Answer Retry Entire Group 9 more group attempts remaining Previous

Organic Chemistry

Ethers Solutions

Thu Dec 2 10:07 PM okmarks Profiles Tab Window Help X Content Bb MestReNova * Update: -xythos.content. blackboardcdn.com/5b6cbef360ea4/15603898?X-Blackboard-Expiration=1638522000000&X-Blackbo... : B Exercise Science 6 Reading List C CHM Textbook + Work Schedule P Home The Prince AU Gmail BIO Textbook NAU Google Drive . 8 / 8 100% + 1.5 1.0 20 3.0 3.5 2.5 11 (ppm) 4.0 7.4 7.0 6.8 73 (ppm) 1 ))) etv s MacBook Air DO NO D FO > O 9 SUN 8 7 3 8 %6 5 $ 4 6 3 P 0 o I 1 Y U T E R J K L G H D F Ş M N. M V - B C V a option command