To apply a new waterproofing membrane on top of an old bitumen waterproofing membrane, the surface of the old membrane should be thoroughly cleaned and prepared. Any loose debris, dirt, or old adhesive should be removed to ensure proper adhesion of the new membrane. Once the surface is clean, a primer should be applied to promote adhesion between the old and new membranes. Finally, the new waterproofing membrane can be installed according to the manufacturer's instructions, ensuring that it is properly sealed and bonded to the old membrane to provide effective waterproofing. **

The solution that is optically inactive but chiral with 4 substituents is a meso compound. A meso compound is a molecule with chiral centers but also has an internal plane of symmetry, which results in the overall molecule being optically inactive. This occurs when the substituents on the chiral centers cancel each other out in terms of their effect on the overall molecule's chirality. Therefore, even though the molecule is chiral, it does not rotate plane-polarized light and is optically inactive. **

A utility knife or a sharp blade is typically used to cut the waterproofing membrane. It is important to use a sharp tool to ensure clean and precise cuts, which will help in achieving a proper seal and prevent water leakage. Care should be taken to avoid damaging the underlying surface while cutting the membrane. **

Ideally, the waterproofing membrane should be applied in dry weather to ensure proper adhesion and effectiveness. If the membrane is applied and then it rains before it has fully cured, it can compromise its ability to create a watertight seal. Water exposure during the curing process can lead to delamination, reduced adhesion, and potential leaks. Therefore, it is best to apply the waterproofing membrane when there is no rain in the forecast and allow it to fully cure before any water exposure. **

In a Fischer projection, the substituents to the left represent the groups that are pointing towards the viewer, while the substituents to the right represent the groups that are pointing away from the viewer. This convention helps to visualize the three-dimensional structure of a molecule in a two-dimensional representation. **

In a Fischer projection, the substituents on the left side represent the vertical bonds, while the substituents on the right side represent the horizontal bonds. This convention helps to easily identify the stereochemistry of the molecule and determine the relative positions of the substituents. The horizontal bonds on the right side are typically pointing towards the viewer, while the vertical bonds on the left side are pointing away from the viewer. **

In a Fischer projection, the substituents that are located to the left are typically the ones with higher priority according to the Cahn-Ingold-Prelog rules, such as groups with higher atomic numbers or multiple bonds. The substituents on the right are usually those with lower priority, like hydrogen atoms or groups with lower atomic numbers. The arrangement of substituents in a Fischer projection helps to determine the stereochemistry of a molecule. **

Trans-2-pentene can have both CH3 substituents below on the same side because the trans configuration refers to the orientation of the two highest priority groups on the double bond, which in this case are the two CH3 groups. In trans-2-pentene, the two CH3 groups are on opposite sides of the double bond, with the other substituents (H atoms) also on opposite sides. This results in a trans configuration, even though the CH3 groups are both below on the same side. **