Yes. Racist it will make it harder to move almost like ooblek
I think it is rarefaction. But im not sure
1,3-pentadiene has two double bonds which are conjugated, which undergo electrophilic addition reaction on reacting with 
.
The structure of 1,3-pentadiene is shown in the image.
When strong acid such as reacts with 1,3-pentadiene, the electrophilic addition reaction can occur either on double bond at 1,2-position or at 3,4-position. The reaction that occurs is shown in the image.
Chloroacetic acid <em>is stronger. </em>
<em>This is because it contains (more electronegative) chlorine atoms in place of (less electronegative) hydrogen atoms.</em>
Nonpolar compound would be symmetrical
