Choice B is correct.
Since all the above compounds are steroids hence their basic skeleton would consist of 17 carbon atoms fused together in the form of 3 six member rings and 1 five member ring , which is illustrated in the option B clearly.
option a is eliminated as none of the steroid has double bond at the position given in option a
option c is eliminated as aldosterone and THG do not mimic the structure shown in option c
option d is eliminated as cholesterol do not have ketone group as that is present in option d
Some examples of steroids are shown here. OCH OH нийт с C= CH CH2 CH2CH CH, CH, CH CHCH2CH2CH2CHCH, HO CH 1 aldoste...
Some examples of steroids are shown here What basic ring structure is common to all steroids?
8. Use the image to answer the questions that follow HO-CH HO-CH2 HO-CH2 CHO H₂o OH CHO CHO OCH CHOICH CH-OH CHCc CHOICH CH 10 | | CH-CH HỒ CH-CH CH-CH CH-CH CH-CH но он но HO он но OH OH HO A B C D Do not e How many carbons does each of the above sugars contain? Name to E n ipo Which sugars are aldoses and which are ketoses? Identify each sugar. Name the linkage for each...
Which of the following reactions will produce the molecule shown below? CH3(CH2)3–0–—CH, CH3 CHCH2)3 + HOẠC–CH2CH, CH2CH2)3-0–CH + H2C-CH3 CH3 (CH2)3-OH + HO—C—CH2CH3 CH3(CH2)3-OH + HC-CH2CH3
Tor F 1. With the exception of steroids, all lipids contain at least one fatty acid. 2. Some lipids contain monosaccharides as part of their structure. 3. Some lipids contain an amino acid as part of their structure. 4. Glycerophospholipids contain a phosphate portion in their structure. 5. All lipids have a molecule of glycerin as their backbone. 6. Polyunsaturated fatty acids have more than one C-C double bond in their "backbone." 7. Fatty acids are soluble in water. 8....
Which of the carbon atoms in the following structure are chiral? ООН ОН HO-CH2-C-CH-CH-CH2-OH 1 2 3 4 5 O carbon atoms: 1 and 5 O carbon atoms: 3 and 4 carbon atoms: 2. 3 and 4 O carbon atoms: 1, 2, 3, 4, and 5
1. The structural formula of 10 compounds listed in Table 1 of this experiment are shown here. ME А B 1 Structure (Letter) Name 2 Acetone 3 Benzaldehyde 4 2-Butanone 5 Heptanal Salicylaldehyde d 6 7 8 Acetophenone Benzaldehyde Cyclohexanone 2-Pentanone 9 10 11 Propanal D = qi.com Od CH3-C-CH . B . D CH, CH CH CH3-CH2-CH2-CH E CHACHA CH, CH, H, OH, OH, - F CH3-CH2-CH2-CH2-CH2-CH2CH Ho CH CHO CH3-CH2-CH2-C-CH H CH3-CH2CH CH ОН
F19 .1 H.CH Erjon HO--- -OH a. 1 6.2 c.3 4.4 24. Which of the following compounds is the enantiome SHO "g compounds is the enantiomer of the structure shown below? HOTH CH₂OH 4. CHO нон ном но-Еннон b. сно с. CH, OH сно 4 сно нон н- он OHH OH CH OHH .CH CH,OH 25. The following two monosaccha howing two monosaccharides form a disaccharide by forming a bond between the two carbons indicated with an asterisk (*). What...
HO CH сн. CH2 нс HC CH3 HAC-HC CH CH CH CH d) OH OH 13. The labels have fallen off three bottles. Bottle A contains a gas, bottle B contains a liquid, and bottle C contains a solid. The labels indicate that the compounds have the same number of carbon atoms, one being an alkane, one an alcohol, and the other a carboxylic acid. Suggest the identity of the contents of each bottle, and give reasons for your explanation...
NADP+ NADPHH HC-OH HO-CH HC-OH нс-ОН CH2OPO;? 6PGDH 'Coz CH OH c=0 HC-OH HC-OH CHOPO3 In pentose phosphate pathway, 6-phosphogluconate undergoes oxidation and decarboxylation by 6- phosphogluconate dehydrogenase (6PGDH) to form D-ribulose 5-phosphate. The reaction generates NADPH, as shown in the scheme. (1) Fill the blanks. During the 6PGDH-catalyzed reaction, the A group of carbon (B) of 6-phosphogluconate is oxidized to the group in ribulose 5-phosphate. A: (name of the functional group). B: (carbon numbering) C: (name of the functional...
CHO 1. NH2OH 2. Ac2o 3. CH,O CHO OH H- HO H HO H HCN H OH OH H- OH H- -OH H- CH2OH CH2OH The Wohl degradation is a series of reactions that shorten an aldose chain by one carbon, it is almost the exact opposite of the Kiliani In this reaction the aldose aldehyde carbonyl group is converted into a nitrile. The resulting cyanohydrin loses HCN under basic cone Conversion of the aldehyde to a nitrile is accomplished...