Примери коришћења Carbons на Енглеском и њихови преводи на Српски
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Those three carbons on the left, that's glycerol.
Short-chain alcohols have alkyl chains of 1-3 carbons.
The burning of fats and carbons is supported by vitamin B5.
Medium-chain alcohols have alkyl chains of 4-7 carbons.
Now the hydrogens and carbons are on opposite sides of the double bond.
These nucleotides are joined together by a bridge of two phosphate groups through the 5' carbons.
Corn syrup here consists of carbons, hydrogens, and oxygens… that we find inside of comets.
The first is like this, where both hydrogens are on same side and both carbons are on the same side.
Flavanols possess two chiral carbons, meaning four diastereoisomers occur for each of them.
Very long chain fatty acids(VLCFA)are fatty acids with aliphatic tails of 22 or more carbons.
The second way is like this.Now the hydrogens and carbons are on opposite sides of the double bond.
Some carbons, under inconceivable heat and pressure, turn into diamonds, and some heavy minerals into other precious stones.
This reaction occurs by hydrolysis with addition of chlorine to one of the carbons and a hydroxyl to the other.
The same reaction can take place between carbons 1 and 5 to form a molecule with a 6-membered ring, called glucopyranose.
Where C-1 is part of an aldehyde group H(C=O)-,and each of the other five carbons bears one hydroxyl group-OH.
It has got same number of hydrogens, carbons, oxygen and same molecular weight but its active life is one day more as compared to Testosterone Caproate.
Therefore, the introduction of oxygen is known to lower the density on nitrogen andenhance substitution at 2-position and 4-position carbons.
Instead of a simple methyl group,the myristoyl group has a tail of 14 hydrophobic carbons, which make it ideal for anchoring proteins to cellular membranes.
Today the term is generally understood in the biochemistry sense, which excludes compounds with only one or two carbons.
The second, branched isomer of butane, isobutane,can connect either at one of the three terminal carbons or at the central carbon, giving rise to another two groups.
Through it's modifications from Nandrolone,it introduces two double-bonds between carbons 11 and 9, and it is this chemical modification that effectively makes Trenbolone totally immune to aromatization(conversion into Estrogen) by way of the aromatase enzyme as well as increasing the strength at which Trenbolone binds to the androgen receptor[2].
As with cyclopropane, the carbon-carbon bonding in the ring has increased p character:the alkene carbons use sp2.68 hybridization for the ring.
Long-chain alcohols(also known as fatty alcohols)have alkyl chains of 8-21 carbons, and very long-chain alcohols have alkyl chains of 22 carbons or longer.[30].
Dexamethasone is based on the cortisol structure butdiffers at three positions(extra double bond in the A-ring between carbons 1 and 2 and addition of a 9-α-fluoro group and a 16-α-methyl substituent).
Each carbon atom bearing a hydroxyl group(-OH), with the exception of the first and last carbons, are asymmetric, making them stereocenter with two possible configurations each(R or S).
Using Le Bel-van't Hoff rule, the aldohexose D-glucose, for example, has the formula(C·H2O)6,of which four of its six carbons atoms are stereogenic, making D-glucose one of 24=16 possible stereoisomers.
Today, the term is generally understood in the biochemistry sense,which excludes compounds with only one or two carbons and includes many biological carbohydrates which deviate from this formula.
Conjugated Linoleic Acid, or CLA,is a term used to refer to a mixture of fatty acids that have the general structure of linoleic acid(18 carbons in length, 2 double bonds) where the double bonds exist two carbons away from each other;