Which of the following is a primary source?

Chemistry

2 answers:

bulgar [2K]2 years ago

6 0

Answer:

I think its C a scientific journal article

Explanation:

Any kind of journal is considered a primary source because journals contain info that the original author wrote. Encyclopedias are considered teritary sources, but im not sure if that counts ...so id go with journals.

7nadin3 [17]2 years ago

4 0

A scientific journal artical

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1,4-Pentadiene has a AHhydro = -254 kJ/mol while trans-1,3-pentadiene has a AHhydra = -226 kJ/mol. Explain this difference in he

julsineya [31]

Answer:

trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.

Explanation:

Here, $\Delta H_{hydro}=H(hydrogenated pdt.)-H(diene)$

H(hydrogenated pdt.) is same for both 1,4-pentadiene and 1,3-pentadiene as they both produce pentane after hydrogenation

H(diene) depends on stability of diene.

More stable a diene, lesser will be it's H(diene) value (more neagtive).

trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.

Hence, $\Delta H_{hydro}$ is higher (less negative) for trans-1,3-pentadiene

5 0

3 years ago

HI(aq)+NaOH(aq)→ <br> what the final balanced chemical equation with the phases included

julia-pushkina [17]

Answer:

$HI(aq)+NaOH(aq)\rightarrow NaI(aq)+H_2O(l)$

Explanation:

Hello there!

In this case, for this neutralization reaction, it is possible to realize that one the neutralization products is water (pH=7) and the other one is the salt coming up from the cation of the NaOH and the anion of the HI:

$HI(aq)+NaOH(aq)\rightarrow NaI+H_2O$

Moreover, since the solubility of NaI is large in water, we infer it remains aqueous whereas the water is maintained as liquid:

$HI(aq)+NaOH(aq)\rightarrow NaI(aq)+H_2O(l)$

Which is also balanced as the number of atoms of all the elements is the same at both sides.

Best regards!

7 0

3 years ago

Draw the structure of the organic product(s) of the grignard reaction between phosgene (clcocl) and excess phenylmagnesium bromi

Jobisdone [24]

Phosgene on reacting with <span>phenylmagnesium bromide generates benzoyl chloride.

Since, </span>phenylmagnesium bromide is added in excess. It would further react with benzoyl chloride to form benzophenone.

Benzophenone on further reacting with phenylmagnesium bromide, and aqueous treatment, gives triphenylmethanol.

Entire reaction pathways is shown below: