Answer:
pent-3-ene-1-yne
Explanation:
1 2 3 4 5
CH ≡ C - CH = CH - CH3
IUPAC name : Pent-3-ene-1-yne
During _<span>A. hydrolysis</span>, bonds between monomers are broken by adding water.
Prefix "hydro-" means water.
"-lysis" - disintegration.
Answer is
C. 2.07 M
For explanation
M1V1 = M2V2
M2 = (M1V1)/V2
M2 = (1.5M x 345ml) / 250 ml
:. M2 = 2.07 M
Answer:
See explanation and image attached
Explanation:
Alkenes undergo hydrogenation to give the corresponding alkanes. Where the structure of the original alkene is unknown, we can deduce the structure of the alkene from the structure of the products obtained when it undergoes various chemical reactions.
Now, the fact that we obtained 2-methylhexane upon hydrogenation and the two compounds had different heats of hydrogenation means that the two compounds were geometric isomers. The original compounds must have been cis-2-methyl-3-hexene and trans-2-methyl-3-hexene.
When reacted with HCl, the same compound C7H15Cl is formed because the stereo chemistry is removed.
However, we know that the trans isomer is more stable than the cis isomer hence the cis isomer always has a higher heat of hydrogenation than the trans isomer. Thus X is cis-2-methyl-3-hexene.
Answer: There would have to be three nitrogen atoms in the products. The law of conservation of matter states that the amount of substance before a reaction occurs should be the same as the amount of substance after the reaction.
Explanation: This is the EXACT sample answer from the test, just reword it if you want. ^