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Nimfa-mama [501]
3 years ago
13

3. If we remember seeing something happen, we can trust that it happened just as we think it did. True or False​

Chemistry
1 answer:
djverab [1.8K]3 years ago
3 0

\huge{ \underbrace{ \overbrace{True}}}

.

\huge\mathfrak\purple{Hope  \: it  \: helps}

Note : Because Many of My Dreams came true and I realized.

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Wassup everyone?????
ioda

Answer:

I'm good

Explanation:

What about you?

4 0
3 years ago
2 bromocyclopentanamine structural formula
Elis [28]

Answer:

The structure is given in attached file.

Explanation:

Explanation

2-bromocyclopentamine (Figure attached) is a synthetic compound which is synthesized by substitution reaction of cyclopentamine and hydrobromide. Its molecular formula and molecular mass are C5H10NBr and 164.05 mol/g respectively.  It is a very reactive compound so it doesn’t available in pure form, it is present in market as a mixture of 2-bromocyclopentamine and Hydrobromide.

Properties :

Its boiling point is 115 0C

Its melting point is – 75 oC

It is highly flammable

It is highly toxic

It is irritant

It is corrosive in nature

5 0
3 years ago
Which Of These Periods Contain Elements With Electrons s,p,d and f orbitals? Periods 1-3 Periods 1-4
Elanso [62]
The answer would be periods 6-7 :)
7 0
3 years ago
Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium diisopropylamide / hexane 2. 1 eq. C
Jobisdone [24]

Answer:

See explanation below

Explanation:

You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.

Now let's analyze what is happening in the reaction so we can predict the final product.

We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.

Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.

Hope this helps

6 0
3 years ago
your mother, who is a self-described chocolate addict, phones you. she has read in the newspaper a summary of a research study s
son4ous [18]

Answer:

This matters because you need to know if this site is crediable

Explanation:

You need to know this because you need to know who runs this site and if it was approved by anything crediable.

7 0
2 years ago
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