Answer:
the answer is Compounds
Explanation:
Compounds are pure substances formed by the combination of elements; they can be decomposed by ordinary chemical means.
fibrous roots; taproots
Explanation:
A taproot root consists of one large main root with smaller roots that branches off into the soil, while the fibrous roots consists of several main roots that branches off to form one mass of roots.
- The root system in plants helps them to absorb water and other nutrients from the soil.
- A taproot is much more like extension of stem that penetrates into the ground.
- It tapers at the end with many other smaller roots branching and networking from it.
- The fibrous root is a series of roots directly from the stem that independent of one another.
- Roots are used by plants for anchorage into the soil.
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Answer:
Metals lose electrons to become cations.
Explanation:
For example, sodium loses an electron to become a sodium cation.
Na· ⟶ Na⁺ + e⁻
A is <em>wrong</em>. Nonmetals gain electrons to become anions.
B is <em>wrong</em>. Metals lose electrons.
D is <em>wrong</em>. Nonmetals gain electrons to become anions.
Answer:
Be
Explanation:
Reactivity increases from left to right and decreases from the top of the column to the bottom of column
Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive. Since soft nucleophiles are less strongly solvated than hard nucleophiles, these solvents boost the relative reactivity of soft anions.
<h3>
Ethanol is either a nucleophile or a base.</h3>
The ethanol is a base Because carbocation is an extremely reactive species, a base or nucleophile as weak as ethanol can replace or remove it. SN1 and E1 would not be conceivable without the carbocation or a strong departing group.
<h3>How do solvents impact anionic nucleophile's reactivity?</h3>
In polar aprotic solvents, nucleophilic substitution reactions of anionic nucleophiles often proceed more quickly. The normal relative reactivity order in such solvents (like DMSO)is Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive.
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