Good conductor of electricity
Answer:
Sofia the firstttdbshsgshaksus
Answer:
B. They are stereoisomers
C. They are enantiomers
Explanation:
Let us consider all the options
A. D and L-glucose are not necessarily furanose, they can also be in free form (open chain) or as a six-membered ring (pyranose)
B. These sugars are stereoisomers as they have the same molecular formula, same bonds but with the different spacial arrangement.
C. Two structures are called enantiomers, if they are stereoisomers and are mirror images of each other and are not-superimposable. The given pair of structures satisfy these conditions
D. Epimers are diastereoisomers (same molecular formula and connectivity having a different spacial arrangement but are not mirror images and non-superimposable) with only one different stereocenter (if there are more than one). This is not the case
E. All monosaccharides (any sugar that cannot be hydrolysed to a simpler sugar) are reducing sugars. So, this option is invalid
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Bronsted-Lowry definition of Bases are Proton acceptors,
or i.e. "A hydrogen ion acceptor"
Answer:
14. (C) -3; 16. B. 0, 3
Explanation:
14. Ionic charge
X: ns²np³.
The element is three electrons short of having a complete octet.
It is likely to react chemically to add those three electrons and form an X³⁻ ion.
16. Orbitals in subshells
The n = 1 shell contains no p orbitals. All the other shells contain three p orbitals.
The n = 1 shell contains only one s orbital. Every higher shell contains a p subshell, and each p subshell contains three p orbitals.