Molecular structure. Isomers have the same formula, so there is the same elements in both. But they have a different molecular structure and when drawn they look different
Answer:
(Most accurate) pippete>graduated cylinder>beaker>balance (Least accurate)
Explanation:
- <em>Most accurate. A pipette prived the most accurate method for delivering a known volume of solution, for example, a 10mL transfer pipette has an accuracy of ±0.02mL</em>
- A graduated cylinder is specifically used to deliver a known volume, its typical accuracy is ±1%, this means that a 100ml graduated cylinder is accurate to ±1mL.
- A beaker is a multipurpose cylindrical glass mainly used to hold liquids. Even though they are graduated, these marks are an estimation, the beaker's accuracy is around 10%.
- Least accurate. A balance measures an object's mass, even though water's density is close to 1, a balance is not the ideal equipment to measure volume, its capacity usually goes between 100-200grams and can measure mass to the nearest ±0.01mg to ±1mg.
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3.37 x 10¹⁰ molecules
Explanation:
Given parameters:
Volume of water = 1pL = 1 x 10⁻¹²L
Density of water = 1.00g/mL = 1000g/L
Unknown:
Number of water molecules = ?
Solution:
To solve this problem, we first find the mass of the water molecule in the inkjet.
Mass of water = density of water x volume of water
Then, the number of molecules can be determined using the expression below:
number of moles = 
Number of molecules = number of moles x 6.02 x 10²³
Solving:
Mass of water = 1 x 10⁻¹² x 1000 = 1 x 10⁻⁹g
Number of moles:
Molar mass of H₂O = 2 + 16 = 18g/mol
Number of moles = 
= 5.6 x 10⁻¹⁴moles
Number of molecules = 5.6 x 10⁻¹⁴ x 6.02 x 10²³ = 33.7 x 10⁹
= 3.37 x 10¹⁰ molecules
Learn more:
Number of molecules brainly.com/question/4597791
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Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
