
Interpretation:
The number of ß-particles that are emitted in 1.0 min from 5.0 mg sample of
Concept introduction:
The nuclear reactions are a type of chemical processes which lead to the formation of some new nuclei with the emission of certain particles. Usually alpha or beta particles, or gamma rays are emitted as a side product with some new daughter nuclei. The nuclei which shows spontaneous decay with time are called as radioactive nuclei. The radioactive decay follows the first order kinetic and the half-life is inversely proportional to the decay constant of the radioactive decay. The radioactive decay follows the first order kinetic and the half-life is inversely proportional to the decay constant of the radioactive decay.

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Chapter 20 Solutions
CHEMISTRY-TEXT
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
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- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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