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soldier1979 [14.2K]
2 years ago
13

Show how to carry out the transformation in the highest yield possible. Select the appropriate reagents and draw the correct org

anic product at each step.
Chemistry
1 answer:
kherson [118]2 years ago
8 0

We want to use this primary leaving group on this primary starting material because it will give us a greater yield and say, if we were to use a secondary reagent in place of this primary.

Now we've moved on from our fundamentals. So we have our starting material and we have That's our beautiful sec futile ether. So now that we've written out are starting material, we can take a thing about where exactly some reactivity may happen. So, for example, could start out with an alcohol that looks as the following. This is a secondary alcohol you can see. So now we need to take a look at some of alcohol.

So now we need to think about our alcohol. Hey, light again. Well, we'll have a hey light. That's a very good leaving group. So we need alcohol. So for example, so now we have a primary structure here, So this will undergo and s and two reaction due to the lacking of hysteric hindrance. Formal negative charge attacks that electrical it carbon bro.

Learn more about Alcohol here-

brainly.com/question/14229343

#SPJ4

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Answer:

C) sp2 and sp2

Explanation:

The hybridization depens on the ammount and type of bonds the atom analized has in the molecule.

For example:

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Analyzing the type and amount of unions of the nitrogen and the carbonyl you will be able to determine the hybridization.

In the imine, the N atom has a double bond to a C and a simple bond two other C, plus the lone pair of electrons (counts as a bond) so it will have a sp2 hybridization.

In the carbonyl, the C has two simple bonds to other C and a double bond to an oxygen atom. It will also have a sp2 hybridization

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