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Identify the bonds that link the isoprene units in α\alpha -farnesene,shown below.How are these units linked: head to head,tail to head or tail to tail?  Identify the bonds that link the isoprene units in  \alpha  -farnesene,shown below.How are these units linked: head to head,tail to head or tail to tail?    \alpha -farnesene α\alpha -farnesene

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Which fatty acid is likely to occur commonly in natural sources? Which fatty acid is likely to occur commonly in natural sources?   A) II B) I and IV C) II and III D) II,III and IV E) V


A) II
B) I and IV
C) II and III
D) II,III and IV
E) V

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Draw the most stable chair conformation of menthol and label each substituent as axial or equatorial.

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11eaa4bc_3e46_903e_9180_67d4a7a153f3_TB5902_00 All substituents are equatorial.

Which of these lipids yields choline upon hydrolysis?


A) A lecithin only
B) A sphingomyelin and a cerebroside
C) A cephalin and a lecithin
D) A cerebroside and a cephalin
E) A lecithin and a sphingomyelin

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E

Choline cannot be found as a product of hydrolysis of any representative of this class of lipids.


A) Cerebrosides
B) Phosphatidylserine
C) Plasmalogens
D) Waxes
E) None of these choices yield choline upon hydrolysis

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The compounds I and II are: The compounds I and II are:   A) Prostaglandins. B) Terpenoids. C) I is a prostaglandin; II is not a prostaglandin. D) I is an E type prostaglandin; II is an F type prostaglandin. E) Both are fatty acids.


A) Prostaglandins.
B) Terpenoids.
C) I is a prostaglandin; II is not a prostaglandin.
D) I is an E type prostaglandin; II is an F type prostaglandin.
E) Both are fatty acids.

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Terpenes are built up from two or more five-carbon units known as ___.

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How many chiral centers does prostaglandin E2 have? Assign R,S configurations to these centers.

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Rank the following fatty acids according to increasing melting point. I: CH3(CH2) 16CO2H II: CH3(CH2) 7CH=CH(CH2) 7CO2H (cis) III: CH3(CH2) 7CH=CH(CH2) 7CO2H (trans) IV: HO2C(CH2) 7CH=CHCH2CH=CH(CH2) 7CH3 (cis,cis)


A) I < II < III < IV
B) IV < III < II < I
C) II < IV < III < I
D) IV < II < III < I
E) IV < I < III < II

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Which of the following could be used to prepare myristic acid,CH3(CH2) 12COOH?


A) CH3(CH2) 11CH2Br,CN-,heat; then H3O+,heat
B) CH3(CH2) 11CH2Br,Mg,(C2H5) 2O; then CO2; then H3O+
C) CH3(CH2) 12CHO,Ag2O,OH-; then H3O+
D) Two of these choices.
E) All of these choices.

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Which of these is a detergent?


A) CH3(CH2) 16COO-Na+
B) [CH3(CH2) 14COO-]2Ca2+
C) CH3(CH2) 10CH2SO3-Na+
D) HOCH2CHOHCH2OH
E) CH3(CH2) 14CH2SH

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Which is not a correct statement concerning naturally occurring triacylglycerols?


A) The greater the degree of unsaturation,the higher the melting point.
B) Saponification yields glycerol and a mixture of carboxylic acid salts.
C) Solid triacylglycerols are termed "fats."
D) Regardless of the exact nature of the R groups,such compounds are water-insoluble.
E) Such compounds frequently are called "triglycerides."

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How many stereogenic centers are there in cholesterol? How many stereogenic centers are there in cholesterol?   A) 2 B) 4 C) 6 D) 8 E) 16


A) 2
B) 4
C) 6
D) 8
E) 16

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The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid? The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)


A) The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)
B) The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)
C) The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)
D) The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)
E) The product of the following reaction sequence is nervonic acid.What is the structure of nervonic acid?   A)    B)    C)    D)    E)

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B

Myelin,the protective coating around nerve fibers,is made up of ___.

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sphingolip...

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The synthesis of cortisone required placing a ketone function at the 11-position of a steroid.Where is position 11? The synthesis of cortisone required placing a ketone function at the 11-position of a steroid.Where is position 11?   A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

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How could you synthesize stearolic acid,CH3(CH2) 7C=C(CH2) 7COOH from oleic acid,CH3(CH2) 7CH=CH(CH2) 7COOH?


A) Br2,CCl4; then 3 NaNH2,heat; then H3O+
B) Li,liq.NH3; then H3O+
C) H2,Pd
D) Peracid; then H3O+; then HA,H2O,heat
E) Excess HCl; then KOH,C2H5OH,heat

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Which of the following statements regarding triacylglycerols is not true?


A) Some undergo autoxidation with oxygen from air.
B) They are solid if they do not have alkene groups.
C) They form lipid bilayers.
D) They form micelles in water.
E) Two of these choices are false statements.

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Salts of long-chain fatty acids are known as ___.

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What is a mixed triacylglycerol?


A) It is a lipid where a terpene is esterifying glycerol
B) It is a triester of glycerol where the acyl groups are identical
C) It is a triester formed by glycerol and acetic acid
D) It is a triester of glycerol where the fatty acids are not all identical
E) It is an ester between glycerol and cholesterol

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