O blood type is recessive hope this helps
Answer:
.. / -.. --- -. - / -.- -. --- .-- / .-- .... .- - / .. / .-- .- ... / - .... .. -. -.- .. -. --. / .-.. . .- ...- .. -. --. / -- -.-- / -.-. .... --- .. .-.. -.. / -... . .... .. -. -.. / -. --- .-- / .. / ... ..- ..-. ..-. . .-. / .- / -.-. ..- .-. ... . / .- -. -.. / .. / .- -- / -... .-.. .. -. -.. / - .... .-. ..- / .- .-.. .-.. / - .... .. ... / .- -. --. . .-. / --. ..- .-.. - / ... .- -.. -. . ... ... / -.-. --- -- .. -. --. / - --- / .... .- ..- -. - / -- . / ..-. --- .-. . ...- . .-. / .. / -.-. .- -. - / .-- .- .. - / ..-. --- .-. / - .... . / -.-. .-.. .. ..-. ..-. / .- - / - .... . / . -. -.. / --- ..-. / - .... . / .-. .. ...- . .-. .-.-.- / .. ... / - .... .. ... / .-. . ...- . -. --. . / - .... .- - / .. -- / ... . . -.- .. -. --. ..--.. / --- .-. / ... . . -.- .. -. --. / ... --- -- --- -. . / - --- / .- ...- . -. --. . / -- . ..--.. / ... - ..- -.-. -.- / .. -. / -- -.-- / --- .-- -. / .--. .- .-. .- -.. --- -..- / .. / .-- .- -. .- / ... . - / -- -.-- / ... . .-.. ..-. / ..-. .-. . . .-.-.-
Explanation:
I think the answer might be nuclear physics
Answer:
Yes. Example: <u>Sulfur hexafluoride (SF₆) molecule</u>
Explanation:
According to the octet rule, elements tend to form chemical bonds in order to have <u>8 electrons in their valence shell</u> and gain the stable s²p⁶ electronic configuration.
However, this rule is generally followed by main group elements only.
Exception: <u>SF₆ molecule</u>
In this molecule, six fluorine atoms are attached to the central sulfur atom by single covalent bonds.
<u>Each fluorine atom has 8 electrons in their valence shells</u>. Thus, it <u>follows the octet rule.</u>
Whereas, there are <u>12 electrons around the central sulfur atom</u> in the SF₆ molecule. Therefore, <u>sulfur does not follow the octet rule.</u>
<u>Therefore, the SF₆ molecule is known as a </u><u>hypervalent molecule</u><u> or expanded-valence molecule.</u>
Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.
