HELP NOW PLEASE URGENT ns <+1421 pts/3400Hideon.HPchces.< Question 17 of 34>Classify each molecule as an aldehyde, ketone, or neither.© Macmillan LearningKetoneNeitherAldehyde0==CHCH,CHCH3iiCH3CH2CHiCH3CH2CCH3OHCH3CHCH3H₁C-O-CH2CH3CH3CH=CHCH3Incorrect AnswerAnswer Bank80Ơ<དDII分F1F2F3F4F5F6F7F8F9

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Answered: ns < +1421 pts /3400 Hide on. HP ch…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.58P

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2 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 T
Acetal and Hemiacetal formation: c. Acetal/hemiacetal CH 3 ty CH H3C [ a. hemiacetal H3C d. Cyclic hemiacetal Gyertych OH Esterification/Amidation: e. Fisher esterification OH + CH₂OH + H3C CH3 H OH + CH3OH H [H*] H₂SO4 H™ a. hemiacetal b.acetal + H₂O
heat CH;CH2CH2CH2CH2CNCH2CH3 + H,0 + HCl CH2CH3
What is the predicted product formed when cyclohexanecarbaldehyde reacts with excess 2-propanol in the presence of sulfuric acid? 01 0 1 0 ||| OIV OV OH OH لیکن پہلی بیٹی || IV
OF OFFICI NSGR my Which of the following aldehydes would be the most soluble in water? (Hint: Remember the relation between the number of carbons in aldehydes and ketones and their solubility in water.) O CH3–CH2–CH2–CH2–CHO O CH3-CH2–CH2–CH2–CH2–CHO O CH3-CH2–CH2–CH2–CH2–CH2–CHO O CH3–CH2–CH2–CHO H f5 % 5 (O & hip 4+ CO fg
Questions 19 and 20
Q10
PRELABORATORY QUESTIONS 1. Consider the following aldehydes and ketones, which you will study in today's experiment. CH3 CH2" | CHg-Ċ–CH3 CH2- CH=CH-C-H -CH2 Cinnamaldehyde Camphor CH3O. .C-H CH3-C-C-CH3 HO Varlin Dlacetyl (2,3-butanedlone) a. Which of the compounds are aldehydes? Which are ketones? b. Which of the aldehydes are aliphatic? Which are aromatic? c. Which compounds would react with Fehling's reagent? With Tollens' reagent? Write equations for all reactions that occur. d. Draw the structural formula of an acetal, formed from one of the aldehydes (your choice), ethyl alcohol, and a trace of acid. e. Which of the compounds would give a positive iodoform test? Write equations for reactions that occur. 2. Draw the structure of the functional for a hemiacetal. group 3. What is evidence for a positive Fehling's test? For a positive Tollens' test?
H2N Present Absent Secondary Amine Amide Heterocyclic Amine Tertiary Amine Primary Amine ZI
Question 2 The reagent which converts a carbonyl group of a ketone into a enamine group is O CH3CH2CH2NHCH3; H3O+ OCH3CH2CH2NH2; OH- O LIAIH[OC(CH3)3]3 O O CH3CH2CH2NHCH3; H+ CH3CH2CH2NH2; H+ C
orgo reaction questions need help.
Question 9 The reagent which converts a carbonyl group of a ketone into a enamine group is O CH3CH2CH2NHCH3; H CH3CH2CH2NH2; H* O CH3CH2CH2NHCH3; H3O* O CH3CH2CH2NH2; OH OLIAIH[OC(CH3)3]3

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