If you take your mom's advice, a. the room will be cooled by minimizing heat transfer by reflection.
The Sun is heating your room by its <em>radiation</em>.
The aluminium foil is shiny, so it reflects the Sun’s radiation back outside the window.
<em>Convection</em> is the transfer of heat caused by the air moving around in your room.
<em>Conduction</em> occurs only when a hot object is in contact with a cooler object.
<h2>Heptene formed is -</h2><h2>

</h2>
Explanation:
The two possibilities when the peroxide is not present
+ HBr →
In presence peroxide,
≡
+ HBr →
- When peroxides are present in the reaction mixture, hydrogen bromide adds to the triple bond of heptane with regioselectivity.
- This reaction is opposite to that of Markovnikov's rule which says that when asymmetrical alkene reacts with a protic acid HX, then the hydrogen of an acid is attached to the carbon with more in number of hydrogen substituents, and the halide (X) group is attached to the carbon with more in number of substituents of alkyl.
- One mole of HBr adds to one mole of 1-heptane.
- The structure of heptene formed is -

Answer:
1,2 dichlorobenzene was used as the solvent for the diels alder reaction: <em>because the co elimination part of the reaction needs high temp and a high boiling point solvent such as 1,2 dichlorobenzene</em>
Explanation:
Diels-Alder Reaction is a useful synthetic tool to prepare cyclohexane rings. It is a process, which occurs in a single step that consists of a cyclic redistribution of its electrons. The two reagents are bond together through a cyclic transition state in which the two new C-C bonds are formed at the same time. For this to occur, most of the time, it is necessary a high temperature and high-pressure conditions. Since 1,2 dichlorobenzene has a boiling point of 180ºC is a good solvent for this type of reactions.
Answer:
CH4 - Methane
B2Si - Diboron monosilicide
N2O5 - Dinitrogen pentoxide
CO2 - Carbon dioxide
Explanation:
When it comes to naming covalent compounds, there are several rules.
The name is derived based on the formula. For example, N2O5. The first element is nitrogen. To the name of the element, you add the prefix that tells us how many of its atoms are in the compound. In this case, there are two atoms, which means that the prefix will be <em>di</em>- (dinitrogen). The second element is oxygen. You are supposed to take only the root of the second element's name and then add the prefix denoting the number of its atoms and the suffix <em>-ide</em> (pentoxide). This is how we'll get dinitrogen pentoxide.
The only exception is methane (CH4), which is an organic compound. Organic compounds are named using the IUPAC nomenclature.