Complete Question:
check the first image for complete part of the question
Answer and Explanation:
Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.
Ring opening of epoxide with acid:
In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)
Ring opening of epoxide with base:
The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.
(check file 2 attached)
Answer:
Combination reaction
Explanation:
N2+H2 = NH3
they combine together to form a product
Because they don't care and think the ozone layer is fine.
Answer:
Conjugate base: Propionate
Explanation:
- Conjugate base contains one less proton as compared to it's parent acid. Deprotonation occurs from most acidic region.
- Propionic acid deprotonates to produce it's strong conjugate base propionate.
- In propionic acid, -OH group in -COOH functional moiety dissociates to produce
. Because the O-H bond electrons remains highly polarized towards oxygen atom due to electron withdrawing inductive effect as well as resonating effect of -COOH moiety.
- Structure of conjugate base has been shown below.
Bohr changed the model of the atom by proposing that electrons travelled in circular orbits with specific energy levels.
