<span>Compare Bromine and Krypton on the basis of their properties, attributes and periodic table facts. Compare elements on more than 90 properties. All the elements of similar categories show a lot of similarities and differences in their chemical, atomic, physical properties and uses. These similarities and dissimilarities should be known while we study periodic table elements. You can study the detailed comparison between Bromine vs Krypton with most reliable information about their properties, attributes, facts, uses etc.</span>
Answer:
They are physical changes.
Explanation:
This is because there in no chemical reaction taking place, just a physical change.
A physical change in a change in which the chemical structure of the substance does not change. Ice, water and steam are all the same on a molecular level, thus changing from ice to water or from water to steam are physical changes.
A chemical change is a change in which the chemical structure of the substance undergoes a change, since this does not happen going for A to B or B to C they are not chemical changes.
Here is the correct question.
Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all lone pairs of electrons.
NF3
SBr2
CCl4
Answer:
Explanation:
The objective here is to draw the molecule three molecules by placing atoms on the grids and connecting them with their respective bonds, therefore including all the lone pairs of electrons.
See the attachment below for the diagrams.
The first compound is know as Nitrogentrifluoride. A non-flammable greenhouse gas. It is majorly used for he production of semi conductors. It has a trigonal planar structure.
SBr2: Sulfur dibromide is a yellowish liquid toxic gas. It results as a reaction between SCl_2 and HBr. Its has a Bent Structure.
CCl_4 : carbon tetrachloride has the presence of a colourless liquid with a sweet smell. Carbon tetrachloride is used for different domestic uses such as: cleaning surfaces, fumigating, cleaning metals etc. It has a tetrahedral structure.
Answer:
See explanation
Explanation:
The reaction of a benzyl bromide with a nucleophile may proceed by SN1 or SN2 mechanism depending on the nature of the solvent used.
Since SN1 reaction involves the formation of a carbocation, it usually predominates in the presence of a poor nucleophiles and protic solvents. Hence when methanol is used as solvent and a poor nucleophile is used, SN1 mechanism predominates.
However, when acetone which is an aprotic solvent is used in the presence of a good nucleophile, SN2 reaction mechanism predominates.
