Answer:
The compound a is 1-methyl cyclohexene (see attachment for structure).
Explanation:
The reaction of 1-Bromo-1-methylcyclohexane with sodium methoxide is a <u>second-order reaction</u> since the <u>methoxide ion is a strong base</u> and also a strong nucleophile. This ion attacks the alkyl halide faster than the alkyl halide can ionize to produce a first-order reaction. However, we can not see the product of nucleophilic substitution. The SN₂ mechanism is blocked due to the <u>impediment of the 1-Bromo-1-methylcyclohexane</u>. The main product, according to the Zaitsev rule, is the 1-methyl cyclohexene, thus forming a <u>double bond</u>.
Then, this cyclohexene is hydrogenated to form the cyclohexane.
Using p1v1/t1=p2v2/t2
p1=50
p2=225
v1=400ml
v2=?
t1=-20=253k
t2=60=333k
50x400/253=225xv2/333
7.9=0.7xv2
v2=7.9/0.7
v2=11.3ml
genetics and reproduction is all about dna.
Answer:
d an attraction between positive ions and electrons