S and S²⁻ do not have the outer subshell fully filled with electrons.
Explanation:
We look at electronic configurations:
Ca 1s² 2s² 2p⁶ 3s² 3p⁶ 4s² - the outer subshell 4s² is fully-filled with electrons
S 1s² 2s² 2p⁶ 3s² 3p⁴ - the outer subshell 3p⁴ is not fully-filled with electrons
Zn²⁺ 1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s⁰ - here the 4s subshell is higher in energy than 3d subshell so will consider 3d¹⁰ the out subshell which is fully-filled with electrons
S²⁻ 1s² 2s² 2p⁶ 3s² 3p² - the outer subshell 3p² is not fully-filled with electrons
Ca²⁺ 1s² 2s² 2p⁶ 3s² 3p⁶ - the outer subshell 3p⁶ is fully-filled with electrons
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electron configurations
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I believe it is C, as helium is one of the lightest noble gases making the particles move faster.
2mm=2,000,000 nm
2,000,000/25=80,000
The answer is 80,000 polio viruses
The Benzenesulfonic acid does not undergo Friedel-Crafts alkylation because of the deactivation of the compound by the carboxylic group.
<h3>What is the Grignard reagent?</h3>
The Grignard reagent is a compound that contains alkyl magnesium halide.
a) The student will be unsuccessful to prepare a Grignard reagent from 4-bromocyclohexanol because of the -OH group that reacts with the Grignard reagent when formed.
b) The Benzenesulfonic acid does not undergo Friedel-Crafts alkylation because of the deactivation of the compound by the carboxylic group.
c) The compound (2S, 3R)- 2,3-Dibromobutane has a specific rotation, [a]D, 0⁰ because it is a meso compound.
d) This is because, the tertiary alkyl halide is more prone to elimination reaction giving the alkene.
e) This is because, the reaction may be occurring by an SN1 mechanism and the rate determining step is the formation of the carbocation.
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