Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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- HO HO. OH base CI EIO- C-OEt epichlorohydrin OH NaOEt 2,6-dihydroxy- acetophenone *Na O2C. .CO2 Na* NaOH, H2O II OH Cromolyn sodium Cromolyn sodium, developed during the 1960s, has been used to prevent allergic reactions primarily affecting the lungs, as, for example, exercised- induced emphysema. It is thought to block the release of histamine, which prevents the sequence of events leading to swelling, itching, and constriction of bronchial tubes. v Cromolyn sodium is synthesized in the above series of steps. rch 31% 11:24 P 4/20/20-arrow_forwardReaction C Select Draw Rings More |||||| C 0 N H 0 || H H₂C C-C I heat H₂C CH–COOH +CH,CH(CH,)NH, H₂C- CH₂ H₂C J Q2Q Draw the amide formed when isopropylamine (CH₂CH(CH³)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. What did I do wrong? N HC- Erase CH₂arrow_forward2 SUPERMARKET23 4 Essay Writing Ser. G calculator - Googl. A Gflights b BATERBLY C CHEGG > KATAPULK CUBA O Maps a AMAZON A Translate Question 6 of 21 Which of the following best describes why only small aldehydes and ketones are soluble in water? A) low molar mass aldehydes and ketones can hydrogen bond through the carbonyl oxygen to water. B) High molar mass aldehydes and ketones have boiling points that are too high to be soluble in water. C) low molar mass aldehydes and ketones hydrogen bond with one another to be soluble in water. D) low molar mass aldehydes and ketones have low boiling points that enhance solubility in water. MacBook Pro 23 2 3 4 7 8 W E R Y F G H. J K Tarrow_forward
- TO 23 #F ** ## 4 .. ||| V Classify each of the molecules below. A B 4 CH3C=C NH₂2 primary amine Osecondary amine O tertiary amine Explanation G Identifying prinary, secondary, and tertiary amines A $ W S not an amine at all MB 4 # @ #D S P D MA C D *** # D # R # *40 O M PRE 6 19 # . PP G 4 CO @ 25 * 4 10 10 # ♥ a # B sh • Check B B => R W # B RS 9 Ra 00 • a B # S 66 D W W PR ** 19 S # 4 4 BA M @ D #** 4 68 # $ D → * ** @ 48 4 9 S B S a #4 NG D B 55 # 46 3 S 62 4 TO 0 # # 9 4 D B 6 19 4 C 99 6 O primary amine O secondary amine O tertiary amine O not an amine at all P C B . 10 S 4 4 * 4 CH3 —CH=CH—NH2 S ## S 9 B B D Ⓡ 46 9 12 . O 16 S W 4 D # a 0 W #4 D D 1 @ 4 d ♥ 30. D # @ a S 12 #D $ B ** * B D S B 00 # 99 * W e A W 1 W S 9 A D * s @ 10 6 66 19 S P P 14 * 0 a 4 A 16 糖 U a V # # A ** DO E C 24 SP ** N $ B a **** @G S D # 4 S -A W C NE # SOP * ## @A 44 • B S * 15 B $ L ** * # W A Or C D # ** 4. $ A 68 B ** $3 RE B O 6 C $ * O * # @@ #D De A 16 8 W N #0 3 @a *** W 慈 B 4 G # ▶ 10 4 BO $…arrow_forward0 0 carboxylic acid CH3CH,CCH2CH3 ester OCH2CH3 anhydride amide CH3CH2CH2CH2CH,COH none of the above CH,CH2CH2CH2CH2CNH2 Cengage Learning | Cengage Technical Support MacBook Airarrow_forwardtaken in order to gor the product Please explain the mechanisms/stepsarrow_forward
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