I2. Draw the structural formula of the organic product when each of the following aldehydes isoxidized to a carboxylic acid.Example:CH,-C-OHEthanalANSWER:a. Pentanalp. Formaldehyde. 3,4-Dichlorohexanal

Aldehydes (RCHO) are oxidised to carboxylic acid (RCOOH).

Answered: 2. Draw the structural formula of the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter16: Synthesis Workshop 1

Section: Chapter Questions

Problem 25CTQ

See similar textbooks

Similar questions

Amines will not react with which of the follow ing? alkyl halides b. carboxylic acids 52. а. с. Ketones d. hydrogen chloride Which statement below is incorrect? the smallest aldehyde has the formula HCOH a carbonyl carbon cons ists of a carbon-oxygen double bond in an aldehyde, the carbonyl carbon is always bonded to a hydrogen atom d. 53. а. b. с. Ketones are more soluble in water than alcohols with the equiva lent number of carbons
The reaction that produced the products below is a:a. dehydrationb. esterificationc. amide synthesisd. hydrolysis (in acid)e. hydrolysis (in base)f. acid baseg. hydrationThe requires starting material must be a(n) :a. carboxylic acidb. esterc. ketoned. amidee. alcoholf. aldehydeg. aromatic
Draw the complete Lewis electron dot structure for dichlorocarbene, :CCl₂. In the reaction of an alkene with dichlorocarbene, the dichlorocarbene is the: a. electrophile. b. Lewis base. The reaction of an alkene with dichlorocarbene is: a. regiospecific. b. Markovnikov. c. nucleophile. c. stereospecific. d. both b and c. d. non-Markovnikov.
Compare aldehydes and ketones as to: (Use acetaldehyde and acetone as examples). A. Reaction with cone. NaOH, heated B. Reaction with phenylhydrazine
1. An alkene reacts with water with an acid catalyst results into a formation of: A. Aldehyde B. Ketone C. Alcohol D. Ester 2. 3-Methylhexanal with K2Cr2O7 will yield: A. 3-Methyl-1-hexanol B. 3-Methylhexanoic acid C. 3-Methyl-1-hexanone D. 3-Methyl-1-hexanethiol 3. This is a reverse process of Hydration reaction: A. Oxidation reaction B. Reduction reaction C. Dehydration reaction D. Hydration reaction 4. Acetic acid reacts with a strong base forms: A. Salt B. Water C. Salt and Water D. No reaction 5. Ketones can be further oxidized with benedict's solution into: A. Alcohol B. Aldehyde C. Catalysts D. No reaction
Phenol is Select one: a. CH3CH2CH2OH b. C8H11OH c. CH3CH2CH2CH2CH2OH d. C6H5OH
Identify the organic functional group of the reactant and the reaction type then predict the functional group(s) of the product(s).The reactant is a(n)a. aromatic ketoneb. aromatic aldehydec. aromatic amided. aromatic alcohole. phenolf. aromatic esterg. aromatic carboxylic acidThe reaction type isa. hydrolysis (in acid)b. hydrolysis (in base)c. amide synthesisd. esterificatione. hydrationf. dehydrationThe product should be a(n)a. carboxlyate ion and aromatic amineb. carboxylate ion and ammonium ionc. carboxylic acid and aromatic alcohold. carboxylic acid and phenole. carboxylic acid and phenoxide ionf. carboxylic ion and aromatic alcohol
Reduction of an alkyl azide results in the formation of —-. A. an imine B. an oxime C. a tertiary amine D. a secondary amine E. a primary amine
1. Cite some reactions in which formaldehyde behaves differently from other aldehydes. 2. Give some biological and medical applications of: a. formalin b. chloral c. urotropine
Draw the structure of the ff. aldehydes and ketones. a. 3-chlorobutanal 6. 8,8-dibromo -4-cthylcyclo hexanone C. 2,4-dimetnylpontanone • Draw the structure of the ff. compounds. a. oyclobutanecarboxylic acid b. 3,8-dimcthylpontancdioic acid C. 4-aminopcntanoic acid d. 2-mothylcycloheranecarooxylic acid m- chlorobėnzoic acid
Q3. Find the acetal carbon (that carbon which was the carbonyl carbon) in each of the following, then draw the carbon and alcohols that could be used to make each of these acetals. a. b. C. d. O O O O O
17. Which functional groups are in the following molecule of aspirin? HO, a benzene ring, an ester, a ketone, and an alcohol b. a benzene ring, two ketones, an ether, and an alcohol a benzene ring, a carboxylic acid, an ether, and a ketone d. a benzene ring, a carboxylic acid, and an ester a. c.

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

General, Organic, and Biological Chemistry

Chemistry

ISBN:

9781285853918

Author:

H. Stephen Stoker

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:

Cengage Learning

General, Organic, and Biological Chemistry

Chemistry

ISBN:

9781285853918

Author:

H. Stephen Stoker

Publisher:

Cengage Learning

Organic And Biological Chemistry

Chemistry

ISBN:

9781305081079

Author:

STOKER, H. Stephen (howard Stephen)

Publisher:

Cengage Learning,

SEE MORE TEXTBOOKS

2. Draw the structural formula of the organic product when each of the following aldehydes is oxidized to a carboxylic acid.