This is true. You are correct
The synthesis of fatty acids starts with a preparratory phase in which acetyl CoA is translocated from mitochondria to the cytosol. However, it cannot pass through the membrane, so it is translocated as citrate that is cleaved to acetyl CoA and oxaloacetate.
In the cytosol, acetyl CoA is transformed to malonyl-CoA, that is, a three carbon compound. Fatty acid synthesis starts with the transfer of the acetyl group from acetyl-CoA to fatty acid synthase.
Two-carbon groups supplied by malonyl-CoA, are supplemented to the developing acyl chain in a series of steps involving condensation, reduction, and dehydration reactions. Elongation of the fatty acid chain ceases at 16 carbon atoms, after 7 cycles, as the free fatty acid is discharged.
It should have the shape number 2.
The substance A has a region that will bind to the nerve cell Y.
The drug developed that's going to block the substance A, will have to have a region that is complementary to the substance A. If those two regions get linked the substance A will have nowhere else to bind.
L believe the answer is C. Hope this helps !
Normally a granite, when metamorphosed, would first form a schist, and then a gneiss would be the higher stage of metamorphism. Presumably in this case, the pressure and temperature conditions were high enough to skip the schist step.