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Agata [3.3K]
3 years ago
9

17 points if you say hi to claim points ur gay.

Chemistry
2 answers:
nikitadnepr [17]3 years ago
6 0

Answer:

hi

Explanation:

Boiling point

skelet666 [1.2K]3 years ago
5 0

Answer:Seriously tho The answer is either boiling point or boiling temperature

Explanation:

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3 years ago
PLEASE SOMEONE! The density of the acetic acid solution is 1.05 g/mL. Calculate the %(m/m) of the acetic acid solution (convert
tigry1 [53]

Answer:

The Percentage concentration of acetic acid = 1.39 %

Explanation:

Density of acetic acid solution = 1.05 g/mL

Volume of acetic acid solution = 0.1 L = 100 mL

From the formula, Density = mass / volume; mass = density × volume

Mass of acetic acid solution = 1.05 g/mL × 100 mL = 105 g

Molar concentration of acetic acid solution = 0.243 mol/L

Molar mass of acetic acid, CH₃COOH = (12 × 2 + 1 ×4 + 16 ×2) = 60 g/mol

From the formula, mass concentration = molar concentration × molar mass

Mass concentration of acetic acid, CH₃COOH = 0.243 mol/L × 60 g/mol = 14.58 g/L

In one liter of acetic acid solution, there are 14.58 g of acetic acid. Therefore, in 0.1 L, there will be 14.58 × 0.1 = 1.458 g of acetic acid.

Percentage concentration of acetic acid = mass of acetic acid / mass of acetic acid solution × 100%

Percentage concentration of acetic acid = (1.458 / 105) × 100% = 1.39 %

The Percentage concentration of acetic acid = 1.39 %

8 0
3 years ago
Aldehydes and ketones are converted into alkenes by means of a direct nucleophilic addition called the Wittig reaction.
zubka84 [21]

Answer:

The given statement- Aldehydes and ketones are converted into alkenes by means of a direct nucleophilic addition called the Wittig reaction, is<u> True.</u>

Explanation:

The Wittig reaction converts aldehydes and ketones into alkenes through a simple nucleophilic addition. A triphenylphosphorine ylide, also known as a phosphorane, reacts with an aldehyde/ketone to produce an oxaphosphetane, a four-membered cyclic intermediate. Instead of being isolated, the oxaphosphetane decomposes spontaneously to release triphenylphosphine oxide and an alkene.

In an SN2 reaction, triphenylphosphine, a good nucleophile, reacts with a primary alkyl halide, followed by deprotonation of the carbon with a solid base, such as butyllithium, to form the ylide. In the product alkene, the carbonyl carbon and the carbon initially bound to the halogen become two carbons with a double bond.

The Wittig reaction's true worth lies in its ability to produce an alkene with a predictable structure, as the C=C bond forms exactly where the C=O bond did in the reactant, with no isomers (other than E/Z isomers) forming.

<u>Hence , the correct option is (A) True.</u>

4 0
3 years ago
Will acid in your stomach will make you unhealthy. do you agree or disagree? explain.
Alex787 [66]
Everyone has acid in their stomach to help digest food.
7 0
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Can boron atoms, B form dative bonds with nitrogen atoms, N in the compound ammonia?​
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"The boron-nitrogen interaction in the studied molecules shows some similarities with the N→B bond in the H3N-BH3 molecule, formally understood as covalent-dative. ... The results show that all the studied BN bonds are triple, since three two-center orbitals have been obtained."

"Formation of a dative bond or coordinate bond between ammonia and boron trifluoride. When the nitrogen donates a pair of electrons to share with the boron, the boron gains an octet. ... In addition, a pair of non-bonding electrons becomes bonding; they are delocalized over two atoms and become lower in energy."

3 0
3 years ago
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