Answer:
its proprionic acid which do not cause any hazardous effect on environment it only effect internal body of human if it is ingested.
Explanation:
Answer:
Lab reports are written to describe and analyse a laboratory experiment that explores a scientific concept. They are typically assigned to enable you to: Conduct scientific research. Formulate a hypothesis/hypotheses about a particular stimulus, event, and/or behaviour.
I Suggest going back in the book to look through what you want to use for your presentation as well as your key details and purpose for writing.
Explanation:
Answer:
Nanometer, micrometer, centimeter, decimeter, dekameter, kilometer
Explanation:
The objects that are rubbed together will create charges among themselves due to friction.
(1) The balloon rubbed with a wool cloth will be charged.
(2) If she comb near a small, uncharged object nothing will change.
(3) This is a scientific investigation because it does not involved a step by step process to answer a scientific query.
Answer:
React it with CH₃MgBr and work up the product with saturated ammonium chloride solution
Explanation:
Grignard reagents convert esters into tertiary alcohols.
The general equation is
![\text{RCOOR}' \xrightarrow[\text{2. H}^{+}]{\text{1. R$^{\prime \prime}$MgBr}}\text{RR$_{2}^{\prime \prime}$C-OH}](https://tex.z-dn.net/?f=%5Ctext%7BRCOOR%7D%27%20%5Cxrightarrow%5B%5Ctext%7B2.%20H%7D%5E%7B%2B%7D%5D%7B%5Ctext%7B1.%20R%24%5E%7B%5Cprime%20%5Cprime%7D%24MgBr%7D%7D%5Ctext%7BRR%24_%7B2%7D%5E%7B%5Cprime%20%5Cprime%7D%24C-OH%7D)
The Grignard reagent in this synthesis is methylmagnesium bromide. You prepare it by reacting a solution methyl bromide in anhydrous ether with magnesium and a few crystals of iodine.
The reaction consumes 3 mol of CH₃MgBr per mole of dimethyl carbonate, and everything happens in the same pot.
Acid workup of the product usually involves the addition of a saturated aqueous solution of ammonium chloride and extraction with a low-boiling organic solvent.
The mechanism involves:
Step 1. Nucleophilic attack and loss of leaving group
(a) The Grignard reagent attacks the carbonyl of dimethyl carbonate, followed by (b) the loss of a methoxide leaving group.
Step 2. Nucleophilic attack and loss of leaving group
(a) A second mole of the Grignard reagent attacks the carbonyl of methyl acetate, followed by (b) the loss of a methoxide leaving group.
Step 3. Nucleophilic attack and protonation of the adduct.
(a) A third mole of the Grignard reagent attacks the carbonyl of acetone, followed by (b) protonation of the alkoxide to form 2-methylpropan-2-ol.