What type of telescope can you use in a bedroom?

Chemistry

1 answer:

Nitella [24]2 years ago

8 0

D
Is the answer because of the ratio of you fart and the smell in ur nose

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Part B

sashaice [31]

The anticodons corresponding to the codons on the mRNA (from part A) is 5' CGA - AAA - GUU 3'.

<h3>What are anticodons?</h3>

Anticodons are nucleotide sequences on tRNA molecules that are complementary to the codons found on mRNA molecules.

The anticodons on tRNA molecules determine the amino acid that is carried by the tRNA.

Just like codons, anticodons occur in triplets of nucleotide sequences.

Considering the codons on the mRNA molecule:

3’ GCT | TTT | CAA | AAA ’5

The complementary anticodon will be:

5' CGA - AAA - GUU 3'

Learn more about anticodons at:brainly.com/question/28067314

#SPJ1

7 0

1 year ago

) If you started with 2.3182 g of 3-nitrophthalic acid and had a 93% yield of 3-nitrophthalhydrazide, how many grams of 3-nitrop

MArishka [77]

Answer: 1.8124 g of 3-nitrophthalhydrazide were recovered.

Explanation:

The balanced chemical reaction will be :

$C_8H_5NO_6+N_2H_4\rightarrow C_8H_5N_3O_4+2H_2O$

moles of 3-nitrophthalic acid = $\frac{\text {given mass}}{\text {molar mass}}=\frac{2.3182g}{211.13g/mol}=0.0110mol$

As 1 mole of 3-nitrophthalic acid gives = 1 mole of 3-nitrophthalhydrazide

0.0110 moles of 3-nitrophthalic acid gives = $\frac{1}{1}\times 0.0110=0.0110$ mole of 3-nitrophthalhydrazide

mass of 3-nitrophthalhydrazide = $moles\times {\text {molar mass}}=0.0110mol\times 177.16g/mol=1.9488g$

As the percentage yield is 93% , the mass of 3-nitrophthalhydrazide recovered = $\frac{1.9488\times 93}{100}=1.8124g$

Therefore 1.8124 g of 3-nitrophthalhydrazide were recovered.

4 0

2 years ago

Rank the compounds in each set in order of increasing acid strength.

Viktor [21]

Answer:

See explanation

Explanation:

For this question, we have to remember the effect of an atom with high electronegativity as "Br". If the "Br" atom is closer to the carboxylic acid group (COOH) we will have an inductive effect. Due to the electronegativity of Br, the electrons of the C-H bond would be to the Br, then this bond would be weaker and the compound will be more acid (because is easier to produce the hydronium ion $H^+$ ).

With this in mind, for A in the last compound, we have 2 Br atoms near to the acid carboxylic group, so, we will have a high inductive effect, then the C-H would be weaker and we will have more acidity. Then we will have the compound with only 1 Br atom and finally, the last compound would be the one without Br atoms.

In B, the difference between the molecules is the position of the "Br" atom in the molecule. If the Br atom is closer to the acid group we will have a higher inductive effect and more acidity.

See figure 1

I hope it helps!