5. Draw a circle around the compound in each horizontal row that is the most basic....
4. Draw a circle around the compound that reacts most rapidly with KOH in water solvent, and draw a rectangle around the compound that reacts most slowly (Ph=phenylCH) in each horizontal row (6 points). There 5. Write the products of the following reactions. If there is no reaction write NR. (26 points, 2 each). 1. SOCI, 2.CH,CH,OH 1. SOCI, 2. (CH,CH, CHL PhầCH OCH CH,OH, catalytie HC Phách, C OOLCH CH, NH, catalytic HCI
Which compound is the most basic? Please give pka values each compound. A B C D NH2 NH2
4 pts) 9. Provide answers to the following questions: a. Draw a circle around the compound of the pair given to the right that has the higher melting point. b. Draw a circle around the compound of the pair given to the right that has the higher boiling point. c. Give the structure of an amine having three carbon atoms that cannot form hydrogen bonds with another molecule of this amine. d. Give the structure of a chlorinated alkane having...
For each of the following pairs of molecules, indicate the compound containing the most basic nitrogen atom For each of the following pairs of molecules, indicate the compound containing the most basic nitrogen atom. NH VS N HN HỌN VS H₂N A с Pair 1: [Select) Pair 2: (Select)
5. With the compounds shown below, draw a rectangle around the compound which is a secondary alcohol. (1 mark) OH OH OH OH OH
with one another? no loan pais 1. For each compound shown below, number the illustrated protons according to their acidity: most acidic (1) to least acidic (3). (9 points) H H NH2 H OH HO F F OH O HS OH 13. Shown below is the formal structure of the amino acid methionine and its structure as it exists at physiological pH ( 7.3). In each case, the molecule itself is neutral; however at pH 7.3 there is an atom...
Multiple Choice (5 points each, 30 points total). Circle the one BEST answer for each problem. 1. Which of the following tertiary alcohols cannot be prepared using the reaction of an ester with excess (2 equivalents) Grignard reagent? . Which of the following esters undergoes hydrolysis in basic conditions (saponification) most readily? . Which compound will be essentially unreactive with excess 1-butanol in acid-catalyzed conditions (upon moderate heating if required)? . Which of the following is the best method for...
For each of the following pairs of molecules, indicate the compound containing the most basic nitrogen atom. NH VS N HN vs HON B с D Pair 1: (Select Pair 2: Select)
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
Identify the most and the least basic compound in each of the following sets. Leave the remaining answer in each set blank. Sodium ethoxide: least Ammonia: a) Sodium acetate: most Sodium p-nitrobenzoate: Sodium benzoate: b) Sodium acetylide: Sodium chloroacetate: Sodium fluoroacetate: c) Sodium acetate: Subrhit Answer Try Another Version 10 item attempts remaining