Answer:
See answer below
Explanation:
To understand this, we need to make the reaction involved with the given configuration. Configuration R means that the substituents of the molecule, the priority order goes clockwise (From heaviest to lightest) so, if an Sn2 is ocurring in the reaction this means that the nucleophile, which in this case, is the sodium ethoxide will attack the molecule in the opposite side of the leaving group (which is the chlorine).
Also when this occurs, as Sn2 is a bimolecular reaction and is held in one step, it occurs an inversion in the configuration of the product. So, it's the innitial reactant was R, then the final product will be S.
The mechanism and product can be watched in the attached picture
Hope this helps.
Catalytic hydrogenation causes the oil to become saturated. So hydrogenated vegetable oil has fewer trans fatty acids and thereby less kinks. The greater the unsaturation (double bonds) the higher is the "kinks" in the fatty acid chains. Hydrogenated vegetable oil have higher melting point causing them to be solids at room temperature such as margarine. In the absence of double bonds (hydrogenated) the fatty acids pack tightly in a crystal lattice. Hydrogenated vegetable oil is likely to clog arteries.
Answer:
2) some fake skin stuff is made to practice sticthces, tattoos, or injections
i dont really know the rest sorry
6) C and 7) C
I hope this helps