It is a 5-carbon sugar. On the 2' carbon, there is only an H-, compared to the -OH found in ribose (hence the name, deoxyribose). -OH groups are found on the 1', 3', and 5' carbons. An oxygen bonds between the 4' and 1' carbons, forming a 5-membered ring.
Pentane has 5 carbon atoms in its structure.
This could be simple sugars - but then it could be a lot of other things too.
It is a pentose sugar as it has 5 carbons
Yes, an aromatic hydrocarbon is a six-carbon ring with alternating single and double bonds. The cool part about an aromatic ring is that the double bonds seem to move between starting at carbons 1, 3 and 5 to starting at 2,4 and 6 then flip back. This makes the ring very stable.
Cycloalkanes are named by indicating the number of carbons in the ring with the prefix "cyclo" followed by the total number of carbons in the molecule. For example, a cycloalkane with six carbons in the ring would be named cyclohexane.
5 carbons
It is a 5-carbon sugar. On the 2' carbon, there is only an H-, compared to the -OH found in ribose (hence the name, deoxyribose). -OH groups are found on the 1', 3', and 5' carbons. An oxygen bonds between the 4' and 1' carbons, forming a 5-membered ring.
The molecular formula is C5 H6 O5 so it it has 5 carbons.
5
5
Assuming free-base, 10: three on each of the unsubsituted benzene carbons, two on /each/ of the unsubstituted carbons on the other ring, one on the other carbon and two on the amine. One more, making eleven, as a salt.
It is a 5-carbon sugar. On the 2' carbon, there is only an H-, compared to the -OH found in ribose (hence the name, deoxyribose). -OH groups are found on the 1', 3', and 5' carbons. An oxygen bonds between the 4' and 1' carbons, forming a 5-membered ring.
Pentane has 5 carbon atoms in its structure.
The prefixes for naming hydrocarbons are based on the number of carbon atoms in the molecule. They include: meth- (1 carbon), eth- (2 carbons), prop- (3 carbons), but- (4 carbons), pent- (5 carbons), hex- (6 carbons), hept- (7 carbons), oct- (8 carbons), non- (9 carbons), dec- (10 carbons).
The pyranose formula for an aldohexose is C6H12O6 and the furanose formula for an aldohexose is also C6H12O6. The difference between them lies in the cyclic structure of the molecule, with pyranose having a six-membered ring and furanose having a five-membered ring.
Ribose, CHO(CHOH)3CH2OH, is an aldopentose with three chiral carbon atoms . .............H O ...............\ // ..........H -- C -- OH .................| ..........H -- C -- OH .................| ..........H -- C -- OH .................| ..........H -- C -- OH .................| ................H