Answer:
This question is incomplete; the complete part is:
A) All cell have a cell wall.
B) All cell arise from pre-existing cells.
C) All cell are capable of photosynthesis.
D) All cell can develop into any other type of cell.
The answer is B
Explanation:
The commonly known universal theory proposed in 1838 took the contribution from three remarkable scientists namely: botanist Matthias Schleiden, anatomist Theodor Schwann and biologist Rudolph Virchow. According to the question, Mathias discovered that all plants are made of cells, Schwann determined that all animals are made of cells while Virchow determined that all living things are composed of cells.
However, in addition to Virchow's discovery, he also discovered and proposed that "All cell arise from pre-existing cells", which till date forms part of the three components of the cell theory. The three parts are:
- Cell is the fundamental and basic unit of all living things.
- All living things are made up of one or more cells
- All cells arise from pre-existing cells
<span>Na2CO3 (aq) + CaCl2H4O2 (aq) = CaCO3 (s) + 2 NaCl (aq) + 2 H2O (l)</span>
Societal law is a rule which stretches out to ones in and by the public
Answer:
The answer is option 3, C5H12 + 8O2 → 5CO2 + 6H2O.
Explanation:
In an exothermic reaction, the energy change(ΔH) will always be a negative value.
For endothermic reaction, the energy change's value is positive.
In the options above, option 1 and 2 are endothermic reaction.
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.
