During an experimental workup procedure, a chemist treated a starting material with NaoH in the solvent acetone `[(CH_(3))_(2)C=O]`, however, the starting material was recovered unreacted. Instead, the chemist isolated a small amount of product A (shown below).
Product A
1. Elemental analysis of product A indicated that it consisted only of carbon, hydrogen, and oxygen.
2. Product A had a molecular weight of 116 g/mol.
3. Product A was a methyl ketone because it gave a positive iodoform test.
4. When product A was treated with `Br_(2)` in `C Cl_(4)`, the red bromine colour persisted, because no carbon-carbon double bonds were present to react with the bromine.
The structure of product A was further confirmed when treatment with hot sulfuric acid resulted in the corresponding dehydration product, product (B)gt
Q. What is the molecular weight of a compound that undergoes an aldol self-condensation reaction to result in a `beta`-hydroxy ketone with a molecular weight of 144?

During an experimental workup procedure, a chemist treated a starting material with NaoH in the solvent acetone [(CH_(3))_(2)C=O] , however, the starting material was recovered unreacted. Instead, the chemist isolated a small amount of product A (shown below). Product A 1. Elemental analysis of product A indicated that it consisted only of carbon, hydrogen, and oxygen. 2. Product A had a molecular weight of 116 g/mol. 3. Product A was a methyl ketone because it gave a positive iodoform test. 4. When product A was treated with Br_(2) in C Cl_(4) , the red bromine colour persisted, because no carbon-carbon double bonds were present to react with the bromine. The structure of product A was further confirmed when treatment with hot sulfuric acid resulted in the corresponding dehydration product, product (B)gt Q. Wihch of the following compounds from the passage will give a positive iodoform test.?

During an experimental workup procedure, a chemist treated a starting material with NaoH in the solvent acetone [(CH_(3))_(2)C=O] , however, the starting material was recovered unreacted. Instead, the chemist isolated a small amount of product A (shown below). Product A 1. Elemental analysis of product A indicated that it consisted only of carbon, hydrogen, and oxygen. 2. Product A had a molecular weight of 116 g/mol. 3. Product A was a methyl ketone because it gave a positive iodoform test. 4. When product A was treated with Br_(2) in C Cl_(4) , the red bromine colour persisted, because no carbon-carbon double bonds were present to react with the bromine. The structure of product A was further confirmed when treatment with hot sulfuric acid resulted in the corresponding dehydration product, product (B)gt Q. Based only on observation 1 and 2, which of the following compounds could have been product A?

During an experimental workup procedure, a chemist treated a starting material with NaoH in the solvent acetone [(CH_(3))_(2)C=O] , however, the starting material was recovered unreacted. Instead, the chemist isolated a small amount of product A (shown below). Product A 1. Elemental analysis of product A indicated that it consisted only of carbon, hydrogen, and oxygen. 2. Product A had a molecular weight of 116 g/mol. 3. Product A was a methyl ketone because it gave a positive iodoform test. 4. When product A was treated with Br_(2) in C Cl_(4) , the red bromine colour persisted, because no carbon-carbon double bonds were present to react with the bromine. The structure of product A was further confirmed when treatment with hot sulfuric acid resulted in the corresponding dehydration product, product (B). Q. When a drop of Br_(2) in C Cl_(4) is added to product B, the resulting solution will ew

During an experimental workup procedure, a chemist treated a starting material with NaoH in the solvent acetone [(CH_(3))_(2)C=O] , however, the starting material was recovered unreacted. Instead, the chemist isolated a small amount of product A (shown below). Product A 1. Elemental analysis of product A indicated that it consisted only of carbon, hydrogen, and oxygen. 2. Product A had a molecular weight of 116 g/mol. 3. Product A was a methyl ketone because it gave a positive iodoform test. 4. When product A was treated with Br_(2) in C Cl_(4) , the red bromine colour persisted, because no carbon-carbon double bonds were present to react with the bromine. The structure of product A was further confirmed when treatment with hot sulfuric acid resulted in the corresponding dehydration product, product (B)gt Q. The aldol self-condensation of acetone is an equilibrium that favours acetone over its condensation product. which of the following experimental modifications is most likely to shift the position of equilibrium towards product A?

What are the starting materials to get 2-methylpropene as the major product?

Strutures of products , Starting materials or reagents

Strutures of products , Starting materials or reagents

Strutures of products , Starting materials or reagents

Strutures of products , Starting materials or reagents