Answer:
Explanation:
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In this case, according to the rules for the oxidation states in chemical reactions, it is possible to realize that lone elements have 0 and since magnesium is in group 2A, it forms the cation Mg⁺² as it loses electrons and oxygen is in group 6A so it forms the anion O⁻²; therefore resulting oxidation numbers are:
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In finding the molarity of a solution, we use the following formula:
What is Molarity?
The number of moles of the solute is calculated by dividing the mass of the solute by its molar mass.
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The molar mass of NH4NO3 and (NH4)3PO4 are 80.043 g/mol and 149.0867 g/mol, respectively.
Therefore, has a molarity of
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Answer:
Uracil
Explanation:
The base that will NOT combine with 2-deoxyribose to form a nucleic acid is Uracil.
2-deoxyribose is a pentose sugar found in the DNA (Deoxyribonucleic acid). It is devoid of oxygen in its 2' position. The bases found in DNA are Adenine, Guanine, Cytosine and Thymine. Adenine, Guanine, and Cytosine are also found in RNA (Ribonucleic acid). Thymine is not present in RNA, it is only found in DNA. The base found in RNA is Uracil which in turn is not present in DNA. The five carbon sugar present in RNA is ribose which combines with Uracil.
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
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Answer: Both store of celluar materials
Explanation:
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