To accurately measure the final volume of a solution in a burette, it is important that you read of the measurement in the lower meniscus like for water and for substances like mercury you read it on the upper meniscus. This is the standard way of reading volumes in laboratory apparatus. Also, it should be that the apparatus standing vertically in a plain surface.
Answer:
See explanation
Explanation:
TLC is a chromatographic method in which the solute is spotted on a plate and the plate is placed in an air tight chamber containing a solvent. The solvent is maintained below the level of the spot. The capillary movement of the solvent through the plate achieves the required separation.
If two spots have Rf values of 0.25 and 0.26 respectively and then the plate was removed from the developing chamber, subsequently, the residual solvent was allowed to evaporate from the plate, and then the plate was returned to the developing chamber.
It will be observed after the second development is complete that the new Rf values will be 0.50 and 0.52 respectively. It will just be as though the second chromatogram picked up from where the first chromatogram stopped.
The particles are atoms, his theory is the atomic theory
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