Answer:
second carbon atom from the end
end carbon atom
Explanation:
Carbohydrates are naturally occurring organic compounds containing carbon, hydrogen and oxygen. The general molecular formula of Carbohydrates is
.
Carbohydrates can be classified based on structures,
Carbohydrates with the structure of alkanals (-CHO) are known as aldose while those of the structure of alkanones (C=O) are known as ketose.
In stereochemistry , D series is a kind of configurational arrangement where the hydroxyl group attaches itself to the right hand side.
Thus; in naturally occurring D series of ketoses, the carbonyl group is found on carbon number <u>second carbon atom from the end </u>whereas in aldoses, the carbonyl group is found on carbon number <u> end carbon atom.</u>
The correct answer for the question that is being presented above is this one: "C. planetesimals ® heavier elements ® inner planets ® protoplanets" The list of the stages of development of the inner planets is this <span>C. planetesimals ® heavier elements ® inner planets ® protoplanets</span>
Answer:
how am i suppose to put it in largest to smallest if u didnt give any numbers
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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Answer: capillary action
Explanation: it occurs when the adhesion forces (attraction between two surfaces or substances) in the liquid are stronger than the cohesion forces (attraction between the same molecule)