1s^2, 2s^2, 2p^6, 3s^2, 3p^6, 3d^5, 4s^1
Chromium is strange because it moves on to the 4s orbital instead of filling the 3d orbital with that last electron. Tricky.
Mark as brainliest if this helped! :)
Answer:
The final volume in mL is 7.14 mL or 7.1 mL.
Explanation:
1.Use Boyle's Law(
). Re-arrange to solve for 
<em> for the final volume.</em>
<em />
<em>2. Plug in values. </em>
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
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Answer:
C: 
Explanation:
we can use the molarity equation
so to find M we plug in what we know, which is 6 moles of NaCl and 2 L of water, which gives us:
