CM₂-0-8-(CM)-CH₂CHOCÁCH||14||CH-O-C CH₂CH=CH-CH=CH-CH₂3Triglycerides can be classified by the number of double bonds present in thehydrocarbon chain. Categorize this triglyceride based on the degree of saturation.11Question 18 of 25CH2-O CH₂}CH₂CH=CH-CH=CH-CH=CH-CH3A) saturatedB) monounsaturatedC) polyunsaturatedD) polysaturatedSubmit ABCH₂OHHHOHEWhich carbon is the anomeric carbon in the structure shown here?OHHOHCH₂OHQuestion 15 of 25DA) AB) BC) CD) DE) ESubmit

A triglyceride has a glycerol backbone in which all the hydroxyl groups are esterified to fatty…

Answered: CH₂-0-0 _-(CH₂)-CH₂ Triglycerides can…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Similar questions

Organic chemistry
An incomplete structure of a porphyrin ring is shown below. The structure is missing three pi bonds and does not show the non-zero formal charges on two atoms. Complete the structure of the porphyrin ring with the missing pi bonds and formal charges. 0 0 +t DC 12⁰ H C N O S F P Cl Br I
:0-H-1--:N-H Hydrogen Bond Which statement best helps explain the formation of the hydrogen bond represented in the figure? A The oxygen has a partial positive charge, and the nitrogen has a partial negative charge. (B) The nitrogen has a partial negative charge, and the hydrogen attached to the oxygen has a partial positive charge.
CH;OH НО OH What is the name of this structure? OH OH alpha-D-gulopryranose O beta-L-gulofuransone O alpha-L-gulofuranose beta-D- gulopyranose
Indicate next to each letter the name of the monomers shown below and write the name of the polymer that is produced from the monomer. H-C-OH HỌ-C-H H-C-OH H-C-OH о- 6 CH₂OH 0=P-O О CH₂ Phosphate H group А: Name of polymer: H- Н Н OH H Sugar Н Н. H Nitrogenous base (adenine) C: 0 НО Name of polymer: H C-C-N CH2 SH Н НИ Н III H-N-С-С-0 +111 НКН н B: Name of polymer: Н 0 0-C-H o Н-С-0² H-C-O H S ННННННННННН Н Н Н LI -CH Н ННННННННННН Н Н Н ITIILE I C-C H ...... С-с-с-с-с-с-с III E .. ННННННННННН Н Н С-С-f 111 1 FE D: I НННННННННННННН No polymer!
Although the first two carbons of fructose and glucose are identical in structure to DHAP and GADP (from glycolysis), DHAP and GADP equilibriate on their in solution to favor the ketone over the aldehyde, while fructose and glucose do not. Why? a)The larger size of the molecule sterically hinders the isomerization b)The larger sugars have more OH groups which hydrogen bond and disrupt isomerization c)The larger sugars cyclize, and there is no carbonyl to isomerize in the cyclic form d)The larger sugars cyclize, and in the cyclic form the hydrogen bonding is very strong e)The larger sugars are less soluble in water than the smaller sugars
Determine the chemical formula for each of the following carbohydrates. Use the ratio for carbohydrates to fill in the missing number in the chemical formula. Example: C3H?O3 = C3H6O3 1:2:1 ratio Carbon 1 x 3 = 3 Hydrogen 2 x 3 = 6 Oxygen 1 x 3 = 3 C6H__O6 C5H__O5 C7H__O7 C4H__O4
Give correct typing answer with explanation
DHA is a fatty acid derived from fish oil and an abundant fatty acid invertebrate brains. Hydrogenation of DHA forms docosanoic acid[CH3(CH2)20CO2H], and ozonolysis forms CH3CH2CHO, CH2(CHO)2 (fiveequivalents), and HCOCH2CH2CO2H. What is the structure of DHA if all double bonds have the Z configuration?
Choose the correct structure for thiamine hydrochloride at pH 10. H3C H3C N NH₂ NH₂ CI- A CI- с CH3 CH3 HCI -OH OO H3C H3C N NH3 NH₂ CI- B D CH3 S CH3 S HCI OH -OH
Which of the following organic compound doesnot dissolve in water? glycerol propane propanoic acid propanol H H-C Н Н H-с-с-с Н- OH HICIH H-C c-c 1 Н OH H -+ Н HICIH H Н H H C C H H OH 5-о-т OH -C-H -H OH
For the following lipid, answer the questions listed below. 0- HC-o (CH)),CH=CH(CH,);CH; H,C-o-c-(CH2);CH=CHCH,CH=CHỊCH,),CH, Is this lipid considered a fat or oil? a. b. How many H2 molecules would be needed to go through a complete hydrogenation reaction? Would the hydrogenated product (after hydrogenation has occurred) have a higher or lower mp than the original starting material? С.

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