Which of the following scientific statements are true and which are false? 1- [ ] Symmetric ethers are generally synthesized by dehydration of alkyne. 2- [ ] 2 molecules of Formaldehyde react together to form Aldol product. 3- [ ] Electrophilic aromatic substitution is the characteristic reactions for alcohols. 4- [ ] The SN1 reaction occurs with inversion of configuration. 5- [ ] In acid dehydration of 2-methyl butanol the major product is 2- methyl-2-butene. 6- [ ] Rate of formation of carbocations follow the order 3˚ > 2˚> 1˚> CH3+ 7- [ ] Hemiacetal produces when one mole of alcohol added to aldehyde. 8- [ ]Cyclohexanol is oxidized to a ketone using Jone's reagent. 9- [ ] Mixture of equal parts of enantiomers is called racemic compound. 10- [ ] E1 describes an elimination reaction in which the rate- determining step is unimolecular and does not involve the alkyl halide.

Chemistry
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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 Which of the following scientific statements are true and                      which   are false? 

1-   [      ] Symmetric ethers are generally synthesized by dehydration of                                alkyne.

2-   [      ] 2 molecules of Formaldehyde react together to form Aldol product.

3-   [      ] Electrophilic aromatic substitution is the characteristic reactions for                     alcohols.

4-   [     ] The SN1 reaction occurs with inversion of configuration.

5-   [     ]  In acid dehydration of 2-methyl butanol the major product is 2-                             methyl-2-butene.

6-   [     ] Rate of formation of carbocations follow the order 3˚ > 2˚> 1˚> CH3+ 

7-   [     ] Hemiacetal produces when one mole of alcohol added to aldehyde.

8-   [     ]Cyclohexanol is oxidized to a ketone using Jone's reagent.

9-   [     ] Mixture of equal parts of enantiomers is called racemic compound.

10- [     ]  E1 describes an elimination reaction in which the rate- determining                       step is unimolecular and does not involve the alkyl halide.

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