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Answer:
We identify nucleic acid strand orientation on the basis of important chemical functional groups. These are the <u>phosphate</u> group attached to the 5' carbon atom of the sugar portion of a nucleotide and the <u>hydroxyl</u> group attached to the <u>3'</u> carbon atom
Explanation:
Nucleic acids are polymers formed by a phosphate group, a sugar (ribose in RNA and deoxyribose in DNA) and a nitrogenous base. In the chain, the phosphate groups are linked to the 5'-carbon and 3'-carbon of the ribose (or deoxyribose) and the nitrogenous base is linked to the 2-carbon. Based on this structure, the nucleic acid chain orientation is identified as the 5'-end (the free phosphate group linked to 5'-carbon of the sugar) and the 3'-end (the free hydroxyl group in the sugar in 3' position).
The most common drugs that aspirin may interact with are: Anti-inflammatory painkillers, such as diclofenac, ibuprofen, indomethacin, and naproxen. Taken with aspirin, these can increase the risk of bleeding. Warfarin, an anticoagulant drug, or a blood thinner, which stops the blood from clotting.
Molecular formula: C8H6N2
Empirical formula: C4H3N
Answer:
the weight of products is is equal the weight of the wood plus the weight of oxygen that was used to burn that wood, so weigh of the product is greater than 10 kilograms.
Explanation:
Conservation of mass (mass is never lost or gained in chemical reactions), during chemical reaction no particles are created or destroyed, the atoms are rearranged from the reactants to the products.
In this example wood (mostly carbon) and oxygen are reactants and carbon dioxide (mostly) is product of reaction.